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 3281–3300 of 38,428 recalls
Recalled Item: Medline custom medical procedure kits labeled as: 1) CATH LAB PACK-LF
The Issue: Custom convenience kits are being recall because the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) NEURO BASIN PACK-LF
The Issue: Custom convenience kits are being recall because the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) OPEN HEART CDS-LF
The Issue: Custom convenience kits are being recall because the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) ENSEMBLE RACHIS-LF
The Issue: Custom convenience kits are being recall because the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) CERVICAL PACK-LF
The Issue: Custom convenience kits are being recall because the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: See DocMan
The Issue: Custom convenience kits are being recall because the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: DEEP BRAIN STIMULATION
The Issue: Custom convenience kits are being recall because the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable
The Issue: Software issues were identified in application version 2.x
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) VP SHUNT CDS
The Issue: Custom convenience kits are being recall because the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable
The Issue: Software issues were identified in application version 2.x
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) MEM MAXILLOFACIAL
The Issue: Custom convenience kits are being recall because the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) MICRODISECTOMY PACK
The Issue: Custom convenience kits are being recall because the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) NASAL PACK
The Issue: Custom convenience kits are being recall because the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) ENDOSCOPIC SKULL BASE
The Issue: Custom convenience kits are being recall because the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) FREE FLAP
The Issue: Custom convenience kits are being recall because the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) CRANI
The Issue: Custom convenience kits are being recall because the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: See DocMan
The Issue: Custom convenience kits are being recall because the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable
The Issue: Software issues were identified in application version 2.x
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: See DocMan
The Issue: Custom convenience kits are being recall because the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) UMC DR. BAKER SUPPLEMENT
The Issue: Custom convenience kits are being recall because the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.