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.

48,770 total recalls
2,392 in last 12 months

Showing 2346123480 of 48,770 recalls

Medical DeviceSeptember 26, 2018· Becton Dickinson & Company

Recalled Item: PCEA ASV Yellow Microbore Recalled by Becton Dickinson & Company Due to The...

The Issue: The products have the potential to leak between the connection of the male...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugSeptember 25, 2018· RXQ Compounding LLC

Recalled Item: Lidocaine 1% + Epinephrine 1:100 Recalled by RXQ Compounding LLC Due to...

The Issue: Subpotent drug: During testing of the retention sample, the firm discovered...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 25, 2018· Baxter Healthcare Corporation

Recalled Item: Levofloxacin Injection in 5% Dextrose Recalled by Baxter Healthcare...

The Issue: Superpotent Drug: High out of specification results for levofloxacin...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodSeptember 25, 2018· Whole Foods Market

Recalled Item: 365 Everyday Value Brand White Corn Chips Recalled by Whole Foods Market Due...

The Issue: Product may contain undeclared milk.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 25, 2018· Pro-Dex Inc

Recalled Item: PRO-DEX Surgical Driver Battery Pack PDBP-001 Series PRO-DEX Battery Pack...

The Issue: Visual particulates within a battery Tyvek pouch. The battery is provided...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· GE Healthcare, LLC

Recalled Item: Giraffe Incubator Carestation. Neonatal incubator. Device sold under the...

The Issue: Potential electric leakage affecting the user.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· GE Healthcare, LLC

Recalled Item: Panda Freestanding Warmer. Device sold under the following product names:...

The Issue: Potential electric leakage affecting the user.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· GE Healthcare, LLC

Recalled Item: Giraffe OmniBed Carestation. Neonatal incubator. Device sold under the...

The Issue: Potential electric leakage affecting the user.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· GE Healthcare, LLC

Recalled Item: Giraffe Warmer. Device sold under the following product names: Giraffe...

The Issue: Potential electric leakage affecting the user.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· GE Healthcare, LLC

Recalled Item: Panda iRes Infant Radiant Warmer. Device sold under the following Recalled...

The Issue: Potential electric leakage affecting the user.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· GE Healthcare, LLC

Recalled Item: Panda Wall Mount warmer. Infant radiant warmer Recalled by GE Healthcare,...

The Issue: Potential electric leakage affecting the user.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 14mm x 30mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 518 Biliary Stent 5mm x 30mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 5mm x 30mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 12mm x 60mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 14mm x 80mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 14mm x 60mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 5mm x 60mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 5mm x 30mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 5mm x 20mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing