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. 2,266 recalls have been distributed to Maine in the last 12 months.
Showing 47041–47060 of 48,770 recalls
Recalled Item: SpiraLok 5.0 w/out Needles with Orthocord Product Number: 222969 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0mm with Panacryl and needles Product Number: 222961 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0 w/Needles with violet and blue Orthocord Product Number:...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0mm with Panacryl without needles Product Number: 222965 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 6.5 w/Needles with violet and blue Orthocord Product Number:...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Recalled by Gynex Corporation Due to The wrong electrical connector...
The Issue: The wrong electrical connector pin was attached to the cord during assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Digital Diagnost-Mobile Detector Holder for Digital Diagnost (Single...
The Issue: The Wireless Portable Detector (WPD) is not fixed securely inside the Mobile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray DPM5 Monitor Recalled by Mindray DS USA, Inc. d.b.a. Mindray North...
The Issue: Mindray has identified an issue with the DPM5 monitors where ST and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Components: ROTULE "913" D=32 Recalled by Wright Medical Technology Inc...
The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATS 3000 Automatic Tourniquet System w/HOSES AND LOP SENSOR Intended...
The Issue: Zimmer is conducting a voluntary removal of some Zimmer A.T.S. 3000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extremity Components: PROTHESE A EXPANSION COMPLETE D=6 LG 12 MM Recalled by...
The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hip Components: INSERT MOBILE "COLLEGIA" TAILLE 58*28 Recalled by Wright...
The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premier Value Fiber Capsules Recalled by Raritan Pharmaceuticals, Inc. Due...
The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leader Fiber Capsules Recalled by Raritan Pharmaceuticals, Inc. Due to...
The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wal-Mucil 100% Natural Fiber Recalled by Raritan Pharmaceuticals, Inc. Due...
The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Equate Fiber Therapy Recalled by Raritan Pharmaceuticals, Inc. Due to...
The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Berkley & Jensen Fiber Capsules Recalled by Raritan Pharmaceuticals, Inc....
The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wal-Mucil Plus Calcium Fiber Capsules Recalled by Raritan Pharmaceuticals,...
The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Best Choice Health Care Recalled by Raritan Pharmaceuticals, Inc. Due to...
The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CVS Pharmacy Fiber Capsules for Regularity Recalled by Raritan...
The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.