Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Spectrum Medical Inc

Spectrum Medical Inc Recalls

All product recalls associated with Spectrum Medical Inc.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

Most Recent

Jan 2026

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 1281–1300 of 21319 recalls

Quantum Perfusion Blood Pump (Spectrum) – fluid leakage (2025)

Their is a potential of fluid leakage from the centrifugal blood pump pump during the priming procedure or during clinical procedures.

Moderate

FDAJan 16, 2025Nationwide• Spectrum Medical Inc

IntelliVue Patient Monitor (Philips) – Alarm Failure (2025)

Potential failure to alarm for "No Device Data" INOP. The device to alarm after a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.

High

FDAJan 15, 2025FL, NC• Philips North America Llc

Sertera Biopsy Device (Hologic) – Needle Separation (2025)

Devices presented a condition in which the inner needle separated from the hub and produced a longer throw of the inner needle or dislodgement.

High

FDAJan 15, 2025

1...63 646566 67...1066

Page 65 of 1066Next

Nationwide

• Hologic, Inc

IntelliBridge EC10 Module (Philips) – alarm failure (2025)

Potential failure to alarm for "No Device Data" INOP. The device to alarm after a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.

High

FDAJan 15, 2025FL, NC• Philips North America Llc

IntelliVue Patient Monitor (Philips) – alarm failure (2025)

Potential failure to alarm for "No Device Data" INOP. The device to alarm after a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.

High

FDAJan 15, 2025FL, NC• Philips North America Llc

Single Use Guide Sheath Kit (Olympus) – radiopaque tip risk (2025)

Potential for the radiopaque tip of the guide sheath component to disassociate and fall off into the patient.

High

FDAJan 15, 2025Nationwide• Olympus Corporation of the Americas

Infinity Central Station (Draeger) – Speaker Malfunction (2025)

Edifier speakers (shipped in or after April 2023) may not annunciate when configured in analog mode which can lead to delayed treatment to the patient.

High

FDAJan 14, 2025Nationwide• Draeger Medical Systems, Inc.

Allura CV20 (Philips) – Safety Issue (2025)

Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

High

FDAJan 13, 2025Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands