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 5661–5680 of 38,428 recalls
Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate
The Issue: Thread form issue for the locking holes in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate
The Issue: Thread form issue for the locking holes in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP Distal Lateral Fibular Plate
The Issue: Thread form issue for the locking holes in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP Distal Lateral Fibular Plate
The Issue: Thread form issue for the locking holes in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP Distal Lateral Fibular Plate
The Issue: Thread form issue for the locking holes in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP Distal Lateral Fibular Plate
The Issue: Thread form issue for the locking holes in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate
The Issue: Thread form issue for the locking holes in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate
The Issue: Thread form issue for the locking holes in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate
The Issue: Thread form issue for the locking holes in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m System
The Issue: The Alinity m System camera detects whether tubes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Durapore Surgical Tape
The Issue: Select lots of the 3M Durapore Surgical Tape,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dr¿ger Perseus A500 Anesthesia Workstation
The Issue: Unexpected shutdown while operating on battery power
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Intracoronary Shunts: a) ClearView¿ 1.00 mm Intracoronary Shunt
The Issue: for unsealed sterile packing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Left Heart Vent Catheters: a) DLP¿ Intracardiac Sump 20 Fr
The Issue: for unsealed sterile packing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Disposable Pressure Display Sets: a) DLP¿ 114.3 cm (45 in)
The Issue: for unsealed sterile packing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Vessel Cannulae: a) DLP¿ 2 mm Vessel Cannula Blunt Tip
The Issue: for unsealed sterile packing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Cardioplegia Adapters: a) DLP¿ 1.8 m (6 ft) Pressure
The Issue: for unsealed sterile packing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic DLP Coronary Ostial Cannulae
The Issue: for unsealed sterile packing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Suction Tubes: a) DLP¿ Suction Tube 6-Fr. Shaft with Frazier Tip
The Issue: for unsealed sterile packing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed
The Issue: Nail system contains an out of specification driver-socket
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.