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. 2,317 recalls have been distributed to Maine in the last 12 months.
Showing 39861–39880 of 48,770 recalls
Recalled Item: Transport Rollator with Padded Seat Recalled by Roscoe Medical Inc Due to...
The Issue: The caster may separate completely from the device frame causing injury to user.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered Screw-Vent Implant Recalled by Zimmer Dental Inc Due to Zimmer...
The Issue: Zimmer Dental is recalling Tapered Screw-Vent Implants because the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Recalled...
The Issue: A recall of the APTUS Ulna Shortening 2.5 instrument was initiated due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spline Twist Implant Recalled by Zimmer Dental Inc Due to Zimmer Dental is...
The Issue: Zimmer Dental is recalling Tapered Screw-Vent Implants because the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuum Acetabular System Trabecular Metal Shell with Multi Holes Recalled...
The Issue: The affected products are missing polar boss threads.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Truvada (200 mg emtricitabine and 300 mg tenofovir disoproxil fumarate)...
The Issue: Presence of Foreign Substance: Truvada was found to contain small red...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens Dimension HB1C Flex reagent cartridge Recalled by Siemens Healthcare...
The Issue: Certain lots of the reagent cartridges show confirmed positive bias...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo SET uSpO2 Cable The Masimo SET uSpO2 Pulse Oximetry Recalled by...
The Issue: Firm has identified a small number of Oximetry Cables with crossed-internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symmetric Total Knee Femoral Components Product Usage: Symmetric Total Knee...
The Issue: Packaging of a device was compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DOPamine Hydrochloride and 5% Dextrose INJ Recalled by Baxter Healthcare...
The Issue: Lack of Assurance of Sterility: A small cut in the solution bag may have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Integra Selector Kit Sterile single use device A bi-lumen Recalled by...
The Issue: Some specific lots of Selector Tubing may potentially leak irrigation fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD-Solis Medication Safety Software Recalled by Smiths Medical ASD, Inc....
The Issue: Smiths Medical has identified an issue with a single batch (Lot Number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coloplast Conveen Urine Collection Leg Bag Recalled by Coloplast...
The Issue: Coloplast is recalling the Conveen Contour Leg Bag due to potential leakage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Healthcare Recalled by Merge Healthcare, Inc. Due to It has been...
The Issue: It has been reported that during use, the SpO2 value displayed on the Hemo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...
The Issue: Failed Tablet/Capsule Specifications: Presence of split or broken tablets.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Extended-Release Tablets Recalled by Sun Pharma...
The Issue: Failed Dissolution Specifications; 12 month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bystolic (nebivolol) tablets Recalled by Forest Pharmaceuticals Inc Due to...
The Issue: Failed Dissolution Specification; at the 6-month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cases of Pillsbury Biscuits Buttermilk 4pk. (6 - 4pk / case) Recalled by...
The Issue: Undeclared Milk ingredient on retail package. In error, individually wrapped...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pillsbury Biscuit Flaky Layers retail 4pk package. Recalled by General...
The Issue: Undeclared Milk ingredient on retail package. In error, individually wrapped...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pilling Knife Handles: a) b) c) Recalled by Teleflex Medical Due to The...
The Issue: The knife handles slot depth is out of specification, so blades may not fit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.