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 2601–2620 of 38,428 recalls
Recalled Item: Hemopore 8cm nasal/sinus temporary wound dressing
The Issue: There is a potential for blister seals on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemopore 2PK nasal/sinus temporary wound dressing
The Issue: There is a potential for blister seals on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasopore Standard 8cm fragmentable nasal dressing
The Issue: There is a potential for blister seals on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasopore 4cm Standard 2PK fragmentable nasal dressing
The Issue: There is a potential for blister seals on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasopore 8cm fragmentable nasal dressing
The Issue: There is a potential for blister seals on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasopore Standard 4cm fragmentable nasal dressing
The Issue: There is a potential for blister seals on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasopore Ex Firm 4cm fragmentable nasal dressing
The Issue: There is a potential for blister seals on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasopore Ex Firm 8cm fragmentable nasal dressing
The Issue: There is a potential for blister seals on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasopore 4cm fragmentable nasal dressing
The Issue: There is a potential for blister seals on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otopore Cylinder Standard outer ear dressings
The Issue: There is a potential for blister seals on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasopore 4cm Standard 2PK fragmentable nasal dressing
The Issue: There is a potential for blister seals on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter TruSystem 7500
The Issue: There is a software issue which causes the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter TruSystem 7500 Hybrid Plus (FC)
The Issue: There is a software issue which causes the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Mobile column TruSystem 7500 U
The Issue: There is a software issue which causes the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Stationary column TruSystem 7500
The Issue: There is a software issue which causes the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter TruSystem 7500 Hybrid (MC)
The Issue: There is a software issue which causes the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter TruSystem 7500 Hybrid (SC)
The Issue: There is a software issue which causes the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Stationary column TruSystem 7500 U
The Issue: There is a software issue which causes the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter TruSystem 7500 Hybrid MR IMRIS
The Issue: There is a software issue which causes the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Operating table column TS7500 MOBIUS
The Issue: There is a software issue which causes the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.