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 2350123520 of 48,770 recalls

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 12mm 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 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 Biliary 518 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 518 Biliary Stent 4mm 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 40mm 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 4mm 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 5mm x 40mm 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 24, 2018· Becton Dickinson & Co.

Recalled Item: BD Max Instrument Recalled by Becton Dickinson & Co. Due to A trend for...

The Issue: A trend for false positive Candida glabrata results has been confirmed. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2018· Becton Dickinson & Co.

Recalled Item: BD Max Instrument Reader Spare Part Recalled by Becton Dickinson & Co. Due...

The Issue: A trend for false positive Candida glabrata results has been confirmed. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2018· Roche Diagnostics Corporation

Recalled Item: Roche Diagnostics URISYS 1100 Urine Analyzer Part Number: 03617556001...

The Issue: Limits of Detection (LoD) for protein, nitrite, leukocytes, and erythrocytes...

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

Class II — Potential Health HazardOngoing
DrugSeptember 21, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Nystatin and Triamcinolone Acetonide Cream Recalled by Dr. Reddy's...

The Issue: Failed stability specifications - An out of specification result was...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2018· Teva Pharmaceuticals USA

Recalled Item: Clozapine Orally Disintegrating Tablets Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Disintegration Specifications: Out-of-specification disintegration...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors Recalled by The...

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER with Manifold Recalled by The Metrix...

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER with Manifold Recalled by The Metrix...

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: ExactaMix Recalled by The Metrix Company Due to Potential for leaking product

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors Recalled by The...

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing