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. 2,518 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,518 in last 12 months

Showing 1106111080 of 48,770 recalls

Medical DeviceAugust 11, 2022· Exactech, Inc.

Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...

The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2022· Exactech, Inc.

Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...

The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...

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

Class II — Potential Health HazardOngoing
DrugAugust 10, 2022· Family Dollar Stores, Llc.

Recalled Item: Colgate Anticavity Fluoride Toothpaste Recalled by Family Dollar Stores,...

The Issue: cGMP deviation: Product held outside of appropriate temperature storage...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2022· Family Dollar Stores, Llc.

Recalled Item: Colgate Anticavity Fluoride Toothpaste Recalled by Family Dollar Stores,...

The Issue: cGMP deviation: Product held outside of appropriate temperature storage...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2022· Family Dollar Stores, Llc.

Recalled Item: Colgate Whitening Mouthwash Recalled by Family Dollar Stores, Llc. Due to...

The Issue: cGMP deviation: Product held outside of appropriate temperature storage...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2022· Family Dollar Stores, Llc.

Recalled Item: Colgate Anticavity Fluoride Toothpaste Recalled by Family Dollar Stores,...

The Issue: cGMP deviation: Product held outside of appropriate temperature storage...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2022· Family Dollar Stores, Llc.

Recalled Item: Colgate Anticavity Fluoride Toothpaste OPTIC WHITE STAIN FIGHTER CLEAN MINT...

The Issue: cGMP deviation: Product held outside of appropriate temperature storage...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2022· Family Dollar Stores, Llc.

Recalled Item: Colgate Anticavity Fluoride Toothpaste Recalled by Family Dollar Stores,...

The Issue: cGMP deviation: Product held outside of appropriate temperature storage...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: PF-Neostigmine Methylsulfate Injection Recalled by Nephron Sterile...

The Issue: CGMP Deviations: Potential for cross-contamination due to product carryover...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: PF-Labetalol HCl Injection Recalled by Nephron Sterile Compounding Center...

The Issue: CGMP Deviations: Potential for cross-contamination due to product carryover...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2022· Nephron Sc Inc

Recalled Item: Ketorolac Tromethamine Injection Recalled by Nephron Sc Inc Due to cGMP...

The Issue: cGMP Deviations: deviations leading to potential cross-contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: PF-0.125% Bupivacaine HCl Injection Recalled by Nephron Sterile Compounding...

The Issue: CGMP Deviations: Potential for cross-contamination due to product carryover...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: Trisodium Citrate 0.5% Solution Recalled by Nephron Sterile Compounding...

The Issue: CGMP Deviations: Potential for cross-contamination due to product carryover...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 10, 2022· Angiodynamics, Inc.

Recalled Item: VenaCure EVLT KIT WITH SPOTLIGHT OPS SHEATH 55CM Ref./ Catalog Recalled by...

The Issue: OPS Fiber packaged within specific VenaCure EVLT Procedure Kits does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2022· Saranas, Inc.

Recalled Item: Early Bird Bleed Monitoring System Introducer Sheath Set Recalled by...

The Issue: Bleed monitoring system device design error, causing the device to not power...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis icono biplane- Model No. 11327600 Artis icono floor- Model No....

The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q floor- Model No. 10848280 Artis Q ceiling- Model Recalled by Siemens...

The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis pheno- Model No. 10849000 Recalled by Siemens Medical Solutions USA,...

The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2022· Hologic, Inc

Recalled Item: The BioZorb LP Marker is an implantable radiopaque marker used Recalled by...

The Issue: Hologic BioZorb LP Marker, (Product number F0221), lot number 22A0RL,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter CLEARLINK System Recalled by Baxter Healthcare Corporation Due to...

The Issue: Firm noted an increase in customer reports of leaks.

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

Class I — Serious Health HazardOngoing