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. 2,301 recalls have been distributed to Maine in the last 12 months.
Showing 43241–43260 of 48,770 recalls
Recalled Item: Mizuho Sugita Titanium Standard Aneurysm Clip II Recalled by Mizuho America,...
The Issue: Specific item numbers form Lots 27-J and 29-J of Sugita T2 Aneurysm Clips....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Juggerknotless Drill Bit Recalled by Biomet, Inc. Due to Investigation...
The Issue: Investigation identified that the design of the drill bit may make the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alprazolam Orally Disintegrating Tablets Recalled by Actavis Elizabeth LLC...
The Issue: Failed Tablet/Capsule Specifications; partial tablet erosion resulting in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ropinirole Recalled by Sandoz, Inc Due to Cross contamination with other...
The Issue: Cross contamination with other products: Sandoz is recalling certain lots of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neurotherm NT2000iX RF Generator Model Number: RFG-NT -2000iX Recalled by...
The Issue: NT2000iX software shipped with the international setting turned on. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Optima CT520 and Optima CT540 Computed Tomography (CT) systems. Recalled...
The Issue: There is an issue with the Manual Film Composer feature on some CT products....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous Peripheral Nerve Block Catheter Kit and Set Continuous Peripheral...
The Issue: A labeling inconsistency was discovered in which the lidstock states that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS CA 125 II Calibrators For use in the calibration Recalled by...
The Issue: Ortho Clinical Diagnostics issued a Product Correction Notification for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Transradial Artery Access products Arrow Transradial Artery Access...
The Issue: There is a risk that the introducer needles packaged within the kits can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes TomoFix Plates The Synthes J5606-C TomoFix Osteotomy System is...
The Issue: A labeling correction was initiated related to the Surgical Technique Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinica Anterior Lumbar Plate (ALP) system Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Spine, Inc. is initiating a correction regarding the Trinica ALP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: White grits packaged in a paper bag labeled in part: Smooth & Creamy...
The Issue: Some Aunt Jemima brand Buttermilk Self-Rising Corn Meal Mix, Quick Grits...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: White grits packaged in a paper bag labeled in part: Smooth & Creamy...
The Issue: Aflatoxins. Some Aunt Jemima brand Buttermilk Self-Rising Corn Meal Mix,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: enGen Track System with enGen Select v5.0 with autoverification enabled...
The Issue: Ortho Clinical Diagnostics issued an Urgent Product Correction Notification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Track System with enGen Custom v3.2.2 (& below) Product The VITROS 5...
The Issue: Ortho Clinical Diagnostics issued an Urgent Product Correction Notification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Implant Holder for Synfix (TM)-LR the Synthes Implant Holder...
The Issue: Complaints were received which described the SynFix LR implant holder...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slim Fortune capsules Dietary Supplement. Each bottle contains 30 capsules....
The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Slim Expert softgel capsules Dietary Supplement. One month supply/ 30...
The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidiy capsules Dietary Supplement. Each bottle contains 30 capsules....
The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexedrine¿ (Dextroamphetamine Sulfate) Spansules¿ Sustained Release Capsules...
The Issue: Failed Dissolution Specifications: Out of Specification (OOS) test results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.