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Spacelabs Healthcare, Ltd. Unit B Foxholes Centre; John Tate Road Hertford United Kingdom

Spacelabs Healthcare, Ltd. Unit B Foxholes Centre; John Tate Road Hertford United Kingdom Recalls

All product recalls associated with Spacelabs Healthcare, Ltd. Unit B Foxholes Centre; John Tate Road Hertford United Kingdom.

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Sep 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–20 of 59 recalls

Sentinel V11 (Spacelabs) – Patient Data Mishandling (2025)

Due to two distinct issues: 1. During patient admission, patient demographic fields may default to those of a previously viewed patient. 2. Systems configured with Resting/Rhythm ECG functionality, under specific navigation conditions, test data intended for one patient may be saved under another patient's record

FDASep 16, 2025Nationwide• Spacelabs Healthcare, Ltd. Unit B Foxholes Centre; John Tate Road Hertford United Kingdom

DVI Display (Spacelabs) – EMI Cable Risk (2025)

Due to display cables used for monitors were not in compliance with electromagnetic interference from inadequately shielded cables which may pose serious risk to patient's safety by interfering with the operation of another electronically sensitive medical device are in use.

FDASep 5, 2025Nationwide• Spacelabs Healthcare, Inc.

Inseego USB8 4G Dongle Kit (Remote Diagnostic) – Outdated Software (2025)

Kit USB flash drive contains outdated software, which could result in reverting patient monitor to outdated software and reintroducing the video laryngoscope issue (related to an August 2023 recall), which could lead to delay in diagnosis, delayed treatment, hypoxia due to unexpected loss of video laryngoscopy and all other monitor measurements during system restart.

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FDAMay 30, 2025Nationwide• Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom

Xhibit Telemetry Receiver (Spacelabs) – Windows Proxy Issue (2024)

Telemetry receiver systems may experience a Windows proxy Issue causing the system to shut down and restart (Offline displayed), lasting approximately 1 to 1.5 minutes, which will cause temporary loss of monitoring. If a clinical event occurred during this period, staff may not detect until the system restarts; necessary clinical intervention could be delayed.

FDANov 25, 2024AL, AK, AZ +41 more• Spacelabs Healthcare, Inc.

Eclipse PRO Holter Recorder (Spacelabs) – Serial Number Error (2024)

Due to a manufacturing error the incorrect device serial number was potentially programmed into the holter recorder. The physical serial number label on the device might not match the serial number programmed into the device.

FDANov 25, 2024AR, CA, CO +19 more• Spacelabs Healthcare, Ltd. Unit B Foxholes Centre; John Tate Road Hertford United Kingdom

Eclipse Mini Holter Recorder (Spacelabs) – Serial Number Error (2024)

FDANov 25, 2024AR, CA, CO +19 more• Spacelabs Healthcare, Ltd. Unit B Foxholes Centre; John Tate Road Hertford United Kingdom

Xhibit Telemetry Receiver (Spacelabs) – System Shutdown Risk (2024)

Telemetry receivers with affected software versions may experience unsolicited system shut down and restart (Offline displayed), lasting approximately 1 to 1.5 minutes, which will cause temporary loss of monitoring. If a clinical event occurred during this period, staff may not detect until the system restarts and necessary clinical intervention could be delayed.

FDANov 25, 2024AL, AR, CO +24 more• Spacelabs Healthcare, Inc.

Tempus LS-Manual Defibrillator (Remote Diagnostic) – incorrect labeling (2024)

Due to incorrect labels applied to devices during servicing. Labels contain the incorrect product name and CAT number.

FDAOct 28, 2024Nationwide• Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom

Space Craft Fifth Wheel (SPACE CRAFT) – Cooktop Backlight Failure (2024)

Fire/Burn Risk

Space Craft MFG (Space Craft) is recalling one Suburban Slide in Range installed in a 2023 S-390 fifth-wheel trailers. The LED backlight circuit board in the cooktop range may fail, causing the board to overheat.

NHTSAAug 16, 2024Nationwide• SPACE CRAFT

Philips Tempus LS Defibrillator (Remote Diagnostic) – ECG Interference (2024)

Simultaneous ECG measurements with multiple devices, including a manual defibrillator, on the same patient may cause electrical noise or interference, which may lead to distortions of the ECG signal; distortions may lead to no or ineffective pacing, or no or inappropriate defibrillation pulse.

FDAMay 9, 2024Nationwide• Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom

Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom: Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-10...

Full screen error message may occur on patient monitors with affected hardware version, either during or after laryngoscopes are unplugged from monitors, informing users a 60-100 second shutdown/restart are required. Error prevents: viewing graphical patient vital signs, sounding of pulse audio tone, visualization of patient airway used during intubation; may lead to treatment delay or hypoxia.

FDAAug 24, 2023AL, AZ, CA +39 more• Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom

A/V Carts (Luxor) – Serious Tip-Over Risk (2023)

This recall involves three cart base models: WT42 "Tuffy" plastic cart; W42/AVJ42/SS-AVJ42 metal cart; and LP-DUO/TPDUOEQ plastic cart. The WT42 "Tuffy" is a 3-shelf plastic cart sold under the brand name H. Wilson "Tuffy" in a variety of colors with different color suffixes after the "WT42" prefix in the item number. The carts have a plastic handle with a logo that reads "the Tuffy" in the center. The W42/AVJ42/SS-AVJ42 cart is 3-shelf adjustable height metal cart. It is also sold under the model number AVJ42 with either a Luxor or H. Wilson logo on the front center of the top shelf, and under the model number SS-AVJ42 with a LineLeader logo on the front center of the top shelf. It is sold in a variety of colors with different color suffixes after the "W42" or "AVJ42" prefixes in the item number. The LP-DUO/TPDUOEQ cart is a 3-shelf adjustable height plastic cart with a push handle on the top shelf. The Luxor logo is stamped on the center of the handle and is a black/dark gray color. Please see below for a chart containing a list of recalled cart models. AV42 LP42LPE-B WT42BUE-B/WTD WT42ORE-N/WTD WTPS42BYME-N AV42B LPDUO-B WT42BUE-N WT42OW WTPS42E-B AVJ42 LPDUOBW-B WT42BUE-N/WTD WT42OW-B WTPS42E-N AVJ42-BY LPDUOE-B WT42BUE/WTD WT42OWBE WTPS42E-P AVJ42-CH LPDUOEBW-B WT42BUNH-B WT42OWE WTPS42G-N AVJ42-GN LPDUOENL-B WT42BY WT42OWE-B WTPS42GE AVJ42-OW LPLDUO-B WT42BY-B WT42P WTPS42GE-B AVJ42-P LPLDUOE-B WT42BY-N WT42P-B WTPS42GE-N AVJ42-RB SS-AVJ42 WT42BYBE WT42P-N WTPS42GYE AVJ42-RD SS-AVJ42-LKB WT42BYE WT42PB WTPS42GYE-B AVJ42-T SS-AVJ42-LKBDL WT42BYE-B WT42PE WTPS42GYE-N AVJ42-U SS-AVJ42KB WT42BYE-B/WTD WT42PE-B WTPS42GYME-B AVJ42-YW SS-AVJ42KB+EPS WT42BYE-N WT42PE-B/WTD WTPS42GYME-N AVJ42-Z SS-AVJ42KB+LAP WT42BYE-N/WTD WT42PE-N WTPS42HG-N AVJ42/C5I SS-AVJ42KB+MM1G WT42BYE/WTD WT42PE-N/WTD WTPS42HGE AVJ42B SS-AVJ42KB+MM2C WT42BYME-N/WTD WT42PE/WTD WTPS42HGE-N AVJ42B-GN SS-AVJ42KB2 WT42BYME/WTD WT42R WTPS42ME-B AVJ42B-RB SS-AVJ42KBDL WT42E WT42R-B WTPS42ME-N AVJ42B-RD SUDMC-42-BK WT42E-B/WTD WT42R-B/WTD WTPS42ORE-B AVJ42B-YW SUDMC-42-RB WT42E-N WT42R-N WTPS42OWE AVJ42BKBDL SUDMC-42-RD WT42E-N/WTD WT42RBE WTPS42OWE-B AVJ42DL SUDMC-42-YW WT42E-P WT42RE WTPS42OWME-B AVJ42DL-RB SUDMC-42DL-BK WT42E-P/WTD WT42RE-B WTPS42P-B AVJ42DL-RD SUDMC-42KB-BK WT42G WT42RE-B/WTD WTPS42PE AVJ42DL-YW SUDMC-42KB-RB WT42G-B WT42RE-N WTPS42PE-B AVJ42KB SUDMC-42KB-RD WT42G-N WT42RNH-B WTPS42PE-N AVJ42KB-BY SUDMC-42KB-YW WT42GBE WT42S WTPS42PME AVJ42KB-CH SUDMC-42KBDL-BK WT42GE WT42TN WTPS42PME-B AVJ42KB-GN SUDMC-42KBDL-RB WT42GE-B WT42TN-B WTPS42PME-N AVJ42KB-LG W42A WT42GE-B/WTD WT42TN-B/WTD WTPS42R-B AVJ42KB-OW W42ABU WT42GE-N WT42TNE WTPS42RE-B AVJ42KB-P W42ABUE WT42GME-B/WTD WT42TNE-B WTPS42RE-N AVJ42KB-RB W42ABUEKB WT42GY WT42TNE-N WTPS42RME-B AVJ42KB-RB/WFSB W42ABUEKBDL WT42GY-B WT42Y WTPS42RME-N AVJ42KB-RD W42ABYEKB WT42GY-B/WTD WT42Y-B WTPS42YE-B AVJ42KB-RD/WFSB W42AE WT42GY-N WT42Y-B/WTD WTPS42YME-N AVJ42KB-T W42AEKB WT42GYBE WT42Y-N WTPS42Z-N AVJ42KB-WH W42AEKBDL WT42GYE WT42YE WTPS42ZE AVJ42KB-WH+2MM W42AG WT42GYE-B WT42YE-B WTPS42ZE-B AVJ42KB-WH+MLAP W42AGE WT42GYE-B/WTD WT42YE-N WTPS42ZE-N AVJ42KB-YW W42AGEKB WT42GYE-N WT42YE/WTD WTPS42ZME AVJ42KB-Z W42AKB WT42GYE-N/WTD WT42Z WTPS42ZME-B AVJ42KB/WFSB W42AR WT42GYE/WTD WT42Z-B WTPS42ZME-N AVJ42KBDL W42ARE WT42GYME-N/WTD WT42Z-B/WTD WTPSLP42BYE-B AVJ42KBDL-BY W42AREKB WT42HG WT42Z-N WTPSLP42BYE-N AVJ42KBDL-GN W42AREKBDL WT42HG-B WT42ZE WTPSLP42E-B AVJ42KBDL-LG W42AY WT42HG-N WT42ZE-B WTPSLP42E-N AVJ42KBDL-RB W42AYE WT42HGE WT42ZE-B/WTD WTPSLP42GE-N AVJ42KBDL-RB/M W42AYEKB WT42HGE-B WT42ZE-N WTPSLP42GYE AVJ42KBDL-RD W42E WT42HGE-B/WTD WT42ZE-N/WTD WTPSLP42PE AVJ42KBDL-YW WT42 WT42HGE-N WT42ZME-B/WTD WTPSLP42PE-B AVJ42KBDL/WFSB WT42-B/WTD WT42ME WT42ZME/WTD WTPSLP42PE-N AVJ42KBN WT42-N WT42ME-B/WTD WTPS42-B WTPSLP42RE-N AVJ42N WT42-P WT42ME-N/WTD WTPS42-BASE WTPSLP42ZE AVJ42N-BY WT42-P/WTD WT42ME-P/WTD WTPS42-N WTPSLP42ZE-B AVJ42N-GN WT42/WTD WT42NH WTPS42-P WTPSLP42ZE-N AVJ42N-OW WT42B WT42NHR-B WTPS42BU-N WTPSP42-B AVJ42N-RB WT42BE WT42OR WTPS42BUE WTPSP42BUE LP42-B WT42BU WT42OR-B WTPS42BUE-B WTPSP42BUE-N LP42BW-B WT42BU-B WT42OR-B/WTD WTPS42BUE-N WTPSP42E-B LP42E-B WT42BU-B/WTD WT42OR-N WTPS42BUME-N WTPSP42E-N LP42EBW-B WT42BU-N WT42ORE WTPS42BY-B WTPSP42E-P LP42LE-B WT42BUBE WT42ORE-B WTPS42BY-N WTPSP42ZE LP42LE-B-FLUTE WT42BUE WT42ORE-B/WTD WTPS42BYE-B WTPSP42ZE-B LP42LP-B WT42BUE-B WT42ORE-N WTPS42BYE-N WTPSP42ZE-N

CPSCApr 13, 2023Nationwide• Luxor Workspaces LLC, of Waukegan, Illinois

Spacelabs Healthcare, Inc.: Ultraview SL (UVSL) Command Module, Model 91496

Command modules will display the following when parameter processing is suspended, depending on software version: 1) Older versions will have waveforms present with no alarms, 2) Newer versions have waveforms absent with no alarms. This may cause clinicians to miss a potentially catastrophic event.

FDAApr 12, 2023Nationwide• Spacelabs Healthcare, Inc.

Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom: Tempus Pro Patient Monitor is a portable vital signs moni...

During internal testing, Regulatory Compliance issues were identified regarding the Monitor and Power Supplies for fluid ingress and basic safety issues.

FDAFeb 23, 2023Nationwide• Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom

Spacelabs Healthcare, Inc.: Xhibit Telemetry Receiver, Model: 96280

Software related alarm escalation defect occurs after approximately 25 days of continuous use. Technical alarm escalation for the following alarms, signal loss, all leads off, low battery, SpO2 sensor off, and signal interference, does not occur in the telemetry receiver as specified. Caregiver may not respond to the initial technical alarm and may not be aware of the continuing technical failure.

FDAMay 31, 2022Nationwide• Spacelabs Healthcare, Inc.

2019 SPACE CRAFT FIFTH WHEEL Recall: EQUIPMENT:RECREATIONAL VEHICLE/TRAILER

Space Craft MFG (Space Craft) is recalling certain 2019-2021 travel, fifth-wheel, and semi-trailers (see recall report for specific model numbers). The adhesive that bonds the vented portion of the window may fail.

NHTSAAug 26, 2021Nationwide• SPACE CRAFT

Spacelabs Healthcare, Ltd. Unit B Foxholes Centre; John Tate Road Hertford United Kingdom: Sentinel V10.x & V11.x, Models: 98200 & 98201 - Product U...

During system upgrade incorrect comments may be added to existing tests. In such instance: Resting ECG and ABP tests which did not contain comments at the time of the upgrade, may have unrelated comments added. Existing comments will not be overwritten or removed. Rhythm ECG Tests may have comments overwritten with unrelated comments. Any tests created after the upgrade are not affected.

FDANov 6, 2020Nationwide• Spacelabs Healthcare, Ltd. Unit B Foxholes Centre; John Tate Road Hertford United Kingdom

Spacelabs Healthcare, Inc.: Xhibit Central, Model No. 96102 - Product Usage: intended...

The firm received reports of loss of audio alarm after a power failure or cable disconnection. The loss of audio for a telemetry patient could delay the recognition of an alarm condition.

FDAAug 30, 2019Nationwide• Spacelabs Healthcare, Inc.

2018 PACE CARGO TRAILER Recall: SUSPENSION:REAR:AXLE:NON-POWERED AXLE ASSEMBLY

LGS Industries Inc (LGS) is recalling certain 2018 Look, Pace, and Cargo Express cargo trailers. The spindle weld on the axle may fail, causing separation of the spindle and pipe.

NHTSAMar 28, 2018Nationwide• PACE

Acyclovir Tablets (Apace KY) - Tablet Mix-up (2018)

Presence of Foreign Tablet/Capsule; cartons labeled to contain Acyclovir tablets may contain Torsemide tablets in some of the blister cavities.

Class IIModerate

FDAFeb 9, 2018Nationwide• Apace KY LLC