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
/
Draeger Medical, Inc.

Draeger Medical, Inc. Recalls

All product recalls associated with Draeger Medical, Inc..

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 23361–23380 of 25000 recalls

Draeger Medical, Inc.: Infinity Docking Station (IDS) (transportable patient mon...

Top cover of assembly may separate. The situation can result in the monitor falling, which could result in an injury to the clinician or patient.

FDANov 17, 2006Nationwide• Draeger Medical, Inc.

Draeger Medical, Inc.: Infinity Docking Station (IDS) Gamma/Gamma XL and Infinit...

Top cover of assembly may separate. The situation can result in the monitor falling, which could result in an injury to the clinician or patient.

FDANov 17, 2006Nationwide• Draeger Medical, Inc.

Draeger Medical, Inc.: Infinity Docking Station (IDS) Delta and Kappa Series pat...

Top cover of assembly may separate. The situation can result in the monitor falling, which could result in an injury to the clinician or patient.

FDA

1...1167 116811691170 1171...1250

Page 1169 of 1250Next

Nov 17, 2006

Nationwide

• Draeger Medical, Inc.

VISX INCORPORATED, A SUBSIDIARY OF AMO INC: Excimer Laser System; WaveScan WaveFront System, Software...

Firm became aware of a significant overcorrection in one eye of a patient who had received a wavefront-guided LASIK treatment at a facility in Germany. The probability of a recurrence of this error was determined to be extremely remote. To ensure that this type of incident will not happen again, a software update was developed.

FDANov 17, 2006Nationwide• VISX INCORPORATED, A SUBSIDIARY OF AMO INC

Dentsply Friadent Ceramed: XiVE S plus Screw Implant D3.0/L11, Model Number 26-0122,...

Sterility of dental implants may be compromised due to cracks in packaging/caps on vials.

FDANov 17, 2006Nationwide• Dentsply Friadent Ceramed

Taylor Desk Lamp (Environmental Lighting) – Shock Hazard (2006)

Fire/Burn Risk

This recall involves "Taylor" model burnished nickel metal desk lamp. The adjustable lamp is 16 to 24.75 inches high with adjustment points at the base, mid-shaft and shade. An "O" logo is engraved on the tube cup under the rotary power switch and the name "OTT-LITE" is engraved on the front of the base. Model number 13Z63BN9 or 13T63BN9 is printed on a black label on the underside of the base.

CPSCNov 16, 2006Nationwide• Environmental Lighting Concepts Inc., of Tampa, Fla.

MRL, Inc., A Welch Allyn Company: Welch Allyn PIC 50 Portable Intensive Care System, Multi-...

Shock Delay:The monitor-defibrillator may display an 'ECG Comm' error message on the display during use, which may prevent or cause an unacceptable delay the delivery of a defibrillation shock. This delay could result in failure to resuscitate the patient.

FDANov 15, 2006Nationwide• MRL, Inc., A Welch Allyn Company

J. Jamner Surgical Instruments, Inc.: JariTrak Table Clamp, 1 inch diameter, vertical post, Cat...

The JariTrak Table Clamp may not securely fasten to the bed rail of the OR table during set up of the retractor system. In the event that the clamp is not securely fastened to the bed rail, the system may move during surgery. The firm received several complaints from hospitals.

FDANov 14, 2006Nationwide• J. Jamner Surgical Instruments, Inc.

Radiometer America Inc: ABL 800 FLEX series blood gas analyzers containing softwa...

Software anomaly. Protein removing program incorporated in the operating software for Versions: V3.833 and V5.24, of the ABL700 and ABL800 Blood Gas Analyzers, may allow for protein build up on the electrode membranes of blood gas analyzers. This condition can influence analyzer results. When the protein removal program is run too frequently, more than once a week, or when running the protein rem

FDANov 13, 2006Nationwide• Radiometer America Inc

Radiometer America Inc: ABL 700 Series blood gas analyzers equipped with Software...

FDANov 13, 2006Nationwide• Radiometer America Inc

K-GUARD Fire Extinguishers (Ansul) – Potential Failure (2006)

Fire/Burn Risk

The recall involves K-GUARD® Wet Chemical, FLAG FIRE® KITCHEN ONE® Wet Chemical, FLAG FIRE® Water and SENTRY® Water Fire Extinguishers manufactured and shipped between May 2003 and September 9, 2005. The recall program involves pick-up tube replacements in the following extinguishers: Brand Model Part Number(s) K-GUARD® Wet Chemical K01-1 430849 (UL) 430850 (ULC) K01-2 432843 (UL) 432848 (ULC) SENTRY® Water W02-1 430847 (English) 430848 (Spanish/English) FLAG FIRE® KITCHEN ONE® Wet Chemical KS-6000 552055 (UL) 552500 (ULC) FLAG FIRE® Water PWS-25G 552050 (UL) 552501 (ULC) Model numbers can be found on the fire extinguisher labels. Affected models meet the following criteria: The year 2004 or 2005 is stamped on the hanger hook attachment on the shell. For 2003 models, information on specific serial numbers included in the recall can be found at www.ansul.com for the K-GUARD Wet Chemical and SENTRY Water extinguishers, or at www.pyrochem.com for the FLAG FIRE and KITCHEN ONE Wet Chemical extinguishers. Contact the firm to determine if your extinguisher is included in this replacement program.

CPSCNov 13, 2006Nationwide• Ansul Incorporated, of Marinette, Wis.

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1; 100V -120V, 15 A (cir...

Improperly adjusting the occlusion setting may result in a pump jam error and pump stoppage.

FDANov 10, 2006Nationwide• Terumo Cardiovascular Systems Corp

Computerized Medical Systems Inc: AccuSeed DS Digital Stepper, an accessory to a prostate r...

The In/Out adjustment knob can be over-turned, ultimately causing the incorrect placement of radioactive seeds in the patient.

FDANov 9, 2006Nationwide• Computerized Medical Systems Inc

DeWalt Framing and Circular Saws – Laceration Risk (2006)

Laceration Risk

This recall involves DeWalt DW378G and DW378GT 7 ¼-inch framing saws with date codes 200301-49 through 200637-49. The model numbers for the framing saws are located on the side of the housing. The date code is located either on the name plate or under the handle near the power cord exit. Circular saws involved in this recall have model number DC300 with date codes 200601-49 through 200637-49. The model number on the circular saw is located on the name plate on the top of the motor housing. The date code on the circular saw is located on the underside of the motor housing. Framing saws marked with a "V" on the underside of the handle near the cord set and circular saws marked with a "V" on the underside of the motor housing or under the handle where the battery is inserted have already been repaired and are not involved in this recall.

CPSCNov 8, 2006Nationwide• DeWalt Industrial Tool Co., of Towson, Md.

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1 Integrated Centrifugal...

Following installation of software version 1.30 in October 2006, the firm confirmed a complaint that the new software caused a discrepancy in the pump speed calculation and caused the pump to stop during clinical use and a ''connect motor'' message to be displayed.

FDANov 8, 2006Nationwide• Terumo Cardiovascular Systems Corp

GE OEC Medical Systems, Inc: The Axcess Cranial Screw (sometimes referred to as the Ax...

GE Healthcare is aware of a few instances where the Axcess Cranial Screw has broken during insertion. There is a possibility that breaking of the screws could lead to a health hazard.

FDANov 8, 2006AL, CA, FL +5 more• GE OEC Medical Systems, Inc

Atrium Medical Corporation: Atrium Express Dry Seal Chest Drain with Sterile Fluid Pa...

Chest drainage tubing incorrectly assembled and may disconnect from patient during use

FDANov 8, 2006Nationwide• Atrium Medical Corporation

Warn ATV Winch Kits – Overheating Risk (2006)

Fire/Burn Risk

This recall involves eight-post contactors used on certain 2,500 to 3,500 lb Warn ATV and Utility Vehicle Winch Kits. The black contactors were sold as a part of winch kits and have a "WARN" logo on the top and bottom of the contactor. Warn part number 62135 is printed on the bottom. Contactors are found on the vehicle attached to the power wires, between the battery and the winch. The contactor has four holes for securing it to the vehicle. A complete listing of winch kit part numbers involved in this recall can be found at www.warn.com

CPSCNov 8, 2006Nationwide• Warn Industries Inc., of Clackamas, Ore.

GE OEC Medical Systems, Inc: The Axcess Cranial Screw (sometimes referred to as the Ax...

GE Healthcare is aware of a few instances where the Axcess Cranial Screw has broken during insertion. There is a possibility that breaking of the screws could lead to a health hazard.

Class IIModerate

FDANov 8, 2006AL, CA, FL +5 more• GE OEC Medical Systems, Inc

Smiths Medical PM, Inc.: BCI 3404 Autocorr Plus Pulse Oximeter/ECG/Respiration Mon...

An error occurred at the board manufacturing site which may affect the following parameters: - An electrical noise observed on the SpO2 pleth waveform generating and displaying erratic heart rates. % SpO2 reading displays dashes. - The ECG waveform may appear noisy, ECG readings appear accurate. -Respiration waveform may appear noisy and the respiration readings will be displayed as dashes.

FDANov 6, 2006PR• Smiths Medical PM, Inc.