Medical Device Recalls
This is our largest category by volume. The FDA tracks recalls for an enormous range of medical devices: implants, pacemakers, insulin pumps, surgical tools, blood glucose monitors, X-ray machines, prosthetics, contact lenses, and home health equipment, among many others. We have records dating back to 2005 and add new ones as the FDA publishes them.
Device recalls can happen because of software bugs, manufacturing defects, bacterial contamination, incorrect labeling, or design flaws that lead to inaccurate results or equipment failure. Class I recalls are the most serious and mean the device could cause injury or death.
Showing 26141–26160 of 38,428 recalls
Recalled Item: SINGLE (1) DISPOSABLE TRANSDUCER KIT WITH 03ML FLUSH DEVICE FOR
The Issue: ICU Medical Inc. has identified a potential for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPEN HEART KIT WITH 03ML FLUSH DEVICE FOR FLETCHER ALLEN HEALTH CARE
The Issue: ICU Medical Inc. has identified a potential for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIFURCATED TRANSPAC¿ 4 WITH 03ML FLUSH DEVICE FOR BUFFALO GENERAL HOSP.
The Issue: ICU Medical Inc. has identified a potential for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transpac¿ 4 kit w/72" Macrodrip¿ Admin Set
The Issue: ICU Medical Inc. has identified a potential for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRANSPAC¿ IV DISPOSABLE TRANSDUCER WITH 4 FT. CABLE EXTENSION AND STOPCOCK
The Issue: ICU Medical Inc. has identified a potential for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRANSPAC¿ IV TRIFURCATED MONITORING KIT 72"
The Issue: ICU Medical Inc. has identified a potential for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRANSPAC¿ IV MONITORING KIT
The Issue: ICU Medical Inc. has identified a potential for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRANSPAC¿ IV BIFURCATED MONITORING KIT 72 INCH
The Issue: ICU Medical Inc. has identified a potential for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RIGHT HEART CATH LAB KIT FOR BAPTIST MEM. HOSP.
The Issue: ICU Medical Inc. has identified a potential for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRANSPAC¿ IV MONITORING KIT WITH SAFESET" RESERVOIR AND BLOOD SAMPLING PORT
The Issue: ICU Medical Inc. has identified a potential for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transpac¿ IV Monitoring Kit
The Issue: ICU Medical Inc. has identified a potential for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transpac¿ IV Trifurcated Monitoring Kit w/84" Safeset" Reservoir
The Issue: ICU Medical Inc. has identified a potential for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M.K. WITH 03ML FLUSH DEVICE FOR DRISCOLL FOUNDATION CHILDRENS HOSP.
The Issue: ICU Medical Inc. has identified a potential for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIPLE PRESSURE KIT WITH 03ML FLUSH DEVICE FOR METHODIST M.C. OF ILLINOIS
The Issue: ICU Medical Inc. has identified a potential for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTCA KIT W/03ML FLUSH DEVICE FOR WILLIAMSPORT HOSP
The Issue: ICU Medical Inc. has identified a potential for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CATH LAB KIT #2 FOR MARY HITCHCOCK MEM. HOSP.
The Issue: ICU Medical Inc. has identified a potential for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transpac¿ IV Monitoring Kit w/03 ml Squeeze Flush and Macrodrip
The Issue: ICU Medical Inc. has identified a potential for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transpac¿ IV Bifurcated Monitoring Kit 48"
The Issue: ICU Medical Inc. has identified a potential for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CATH LAB KIT FOR BAPTIST M. C.
The Issue: ICU Medical Inc. has identified a potential for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement floor locking cylinders for the Schaerer model 7300 surgical
The Issue: The floor locking cylinders are contained in the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.