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. 978 recalls have been distributed to Maine in the last 12 months.
Showing 30901–30920 of 48,770 recalls
Recalled Item: Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit...
The Issue: Products are not designed, qualified, manufactured, and/or managed under a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: A problem can occur with the small light marker windows, used for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Offset Reamer Handle Recalled by Greatbatch Medical Due to On June 14, 2016,...
The Issue: On June 14, 2016, Greatbatch discovered a significant increase in the number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: A problem can occur with the small light marker windows, used for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HCG (Chorionic Gonadotropin Lyopholized) II Recalled by Town and Country...
The Issue: Subpotent Drug: due to failed potency results of 74% (spec. 80-125%).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zeasorb AF (miconazole nitrate) Recalled by GSK Consumer Healthcare Due to...
The Issue: Labeling Not Elsewhere Classified: front labels have the incorrect NDC or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Covidien Precision Specimen Container- 4 oz (118 mL) Recalled by Covidien...
The Issue: Sterility of the outer surface of the container compromised due to packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReShape Integrated Dual Balloon System Recalled by Reshape Medical Inc Due...
The Issue: ReShape Medical is recalling the Integrated Dual Balloon System Gen 1 due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Inlay Optima¿ Multi-Length Ureteral Stent Coated Double Pigtail...
The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Totalis Recalled by C.R. Bard, Inc. Due to Labeling: Statement was added to...
The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD INLAY Ureteral Stent with Suture Recalled by C.R. Bard, Inc. Due to...
The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Fluoro-4 Silicone Ureteral Stent Recalled by C.R. Bard, Inc. Due to...
The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olanzapine tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: due to out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Succinylcholine Chloride Recalled by Pharmedium Services, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility: A portion of the batch quantity was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Algerbrush-II Product Usage: Medical - For surgeons to use in Recalled by...
The Issue: According to firm ( Bausch & Lomb, Inc. ) on June 17, 2016 a packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GAMBRO Capillary Dialyzer Recalled by Baxter Healthcare Corp. Due to...
The Issue: Potential presence of particulate matter on the blood side of the dialyzer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage Total 5 Control Level 1 Recalled by Alere San Diego, Inc. Due...
The Issue: Encoded with incorrect ranges that are not consistent with the ranges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ben & Jerrys Brownie Batter Core Ice Cream One Pint Recalled by Unilever...
The Issue: Certain pints of Ben & Jerrys Brownie Batter Core Ice Cream may contain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Roland¿ Preserved Lemons Recalled by Roland Foods, LLC. Due to Undeclared...
The Issue: The product contains undeclared sulfites based on sampling and analysis by...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RF MultiGen¿ Recalled by Stryker Instruments Div. of Stryker Corporation Due...
The Issue: Stryker Instruments is voluntarily recalling the Care...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.