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 17901–17920 of 38,428 recalls
Recalled Item: VANTEX 7FR
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORT AND IO ACCESS DRESSING KIT DT15780A
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CENTRAL LINE BUNDLE ECVC6375
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IV KIT - SORBAVIEW IVS3475
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAP BUNDLE KIT DYNDC2137
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PEDIATRIC PICC INSERTION TRAY CVI4450
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CENTRAL VENOUS ACCESS DEVICE BUNDLE ECVC2840
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Intubation Fiberscope
The Issue: The action is being initiated due to intubation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Connected OR Cart
The Issue: There is a potential problem with firm s
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow JACC with Chlorag+ard Technology Jugular Axillo subclavian Central...
The Issue: Lidstock states the incorrect expiration date for the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrowg+ard Blue Advance JACC Product Code: CDC 42063 JX1A
The Issue: Lidstock states the incorrect expiration date for the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow PICC with Chlorag+ard Technology Product Code: CDA 45041 HPK1A
The Issue: Lidstock states the incorrect expiration date for the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ JACC with Chlorag+ard¿ Technology Jugular Axillosubclavian Central...
The Issue: Lidstock states the incorrect expiration date for the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ JACC with Chlorag+ard Technology Product Code:JR 42563 HPHNM
The Issue: Lidstock states the incorrect expiration date for the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ PICC Kit Product Code: ASK 45541 LVH1
The Issue: Lidstock states the incorrect expiration date for the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrowg+ard Blue Advance PICC pre loaded with Arrow¿ VPS" Precision
The Issue: Lidstock states the incorrect expiration date for the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP Precision Integrated System 120V
The Issue: 2.5A slow blow fuses may have been installed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow PICC Kit Product Code: ASK 45541 RWJ4
The Issue: Lidstock states the incorrect expiration date for the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow PICC with Chlorag+ard Technology Product Code: CDA 45052 HPK1A
The Issue: Lidstock states the incorrect expiration date for the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ PICC with Chlorag+ard¿ Technology Product Code: PR 45552 HPHNL
The Issue: Lidstock states the incorrect expiration date for the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.