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. 2,437 recalls have been distributed to Maine in the last 12 months.
Showing 17341–17360 of 27,655 recalls
Recalled Item: RED SEXP DSTL FEM 19CM RT ASSY Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humeral Guide Wire Ball Tip 2.4 mm Diameter 70 cm Length Recalled by Zimmer...
The Issue: The design verification for the previous packaging configuration G928 does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter Recalled by...
The Issue: The design verification for the previous packaging configuration G928 does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COMP 12MM HUM FRAC STEM MACRO Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...
The Issue: The firm is recalling product that has the potential to not function during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...
The Issue: The firm is recalling product that has the potential to not function during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...
The Issue: The firm is recalling product that has the potential to not function during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter Recalled by...
The Issue: The design verification for the previous packaging configuration G928 does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHO POR FMRL NC 9X125 Recalled by Zimmer Biomet, Inc. Due to Possibility...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RED SEXP DSTL FEM 19CM LT ASSY Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...
The Issue: The firm is recalling product that has the potential to not function during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN Intramedullary Fixation Humeral Guide Wire - Bullet Tip 2.4 Recalled by...
The Issue: The design verification for the previous packaging configuration G928 does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSS CEMENTED IM STEM 12X150 Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...
The Issue: The firm is recalling product that has the potential to not function during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CER BIOLOXD OPTION HD 32MM Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COMP PRIMARY STEM 8MM MINI Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lateral Troch Plate Full Crimp - 254mm Recalled by Zimmer Biomet, Inc. Due...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN Intramedullary Fixation Humeral Guide Wire - Smooth 2.4 mm Recalled by...
The Issue: The design verification for the previous packaging configuration G928 does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim 5 Elite Recalled by St. Jude Medical, Inc. Due to The firm...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension Recalled...
The Issue: Customer complaint of a cut in the side of the leg bag, indicating a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.