Product Recalls in Maine
Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,392 recalls have been distributed to Maine in the last 12 months.
Showing 21801–21820 of 48,770 recalls
Recalled Item: STERILE CAP CHANGE KIT DYNDC1946B Recalled by Centurion Medical Products...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIPLE LUMEN BUNDLE KIT ECVC1540 Recalled by Centurion Medical Products...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSA PORT KIT DYNDC1840F Recalled by Centurion Medical Products...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UVC TRAY UVT875 Recalled by Centurion Medical Products Corporation Due to...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IV START KIT IV8440 Recalled by Centurion Medical Products Corporation Due...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VANTEX 7FR Recalled by Centurion Medical Products Corporation Due to Firm...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORT AND IO ACCESS DRESSING KIT DT15780A Recalled by Centurion Medical...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CENTRAL LINE BUNDLE ECVC6375 Recalled by Centurion Medical Products...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IV KIT - SORBAVIEW IVS3475 Recalled by Centurion Medical Products...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAP BUNDLE KIT DYNDC2137 Recalled by Centurion Medical Products Corporation...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PEDIATRIC PICC INSERTION TRAY CVI4450 Recalled by Centurion Medical Products...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CENTRAL VENOUS ACCESS DEVICE BUNDLE ECVC2840 Recalled by Centurion Medical...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Intubation Fiberscope Recalled by Karl Storz Endoscopy Due to The...
The Issue: The action is being initiated due to intubation scopes improperly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium 4000 Recalled by D.B.P. Distribution Due to Undeclared Sildenafil
The Issue: Marketed without an approved NDA/ANDA: undeclared sildenafil and tadalafil.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate Injection Recalled by Akorn Inc Due to Failed...
The Issue: Failed impurities/degradation specification: Out of Specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stryker Connected OR Cart Recalled by Stryker Corporation Due to There is a...
The Issue: There is a potential problem with firm s Connected OR Cart, 120V resulting...
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 product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrowg+ard Blue Advance JACC Product Code: CDC 42063 JX1A Recalled by Arrow...
The Issue: Lidstock states the incorrect expiration date for the product
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 product
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 product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.