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. 2,371 recalls have been distributed to Maine in the last 12 months.
Showing 25381–25400 of 48,770 recalls
Recalled Item: microTargeting" STar" Drive System (Motorized) Recalled by FHC, Inc. Due to...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" Drive System Distributed by Medtronic Recalled by FHC, Inc....
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" Drive System Recalled by FHC, Inc. Due to The FHC Depth Stop...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" Drive System Recalled by FHC, Inc. Due to The FHC Depth Stop...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" STar" Drive System (Manual) Recalled by FHC, Inc. Due to The...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" STar" Drive System (Manual) Distributed by Medtronic...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outer Package Label: Tapered Screw-Vent Implant System Recalled by Zimmer...
The Issue: Dental implants have incorrect item/lot numbers and size on the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rio System Irrigation Clip - Catalog # 111690 Product Usage: Recalled by...
The Issue: Out of tolerance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hyalomatrix Recalled by Anika Therapeutics, Inc. Due to Hyalomatrix products...
The Issue: Hyalomatrix products are susceptible to degradation as a result of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products PHYT Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: There is a potential for imprecise results when using the slides. Increase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImagePilot Recalled by Konica Minolta Medical Imaging USA, Inc. Due to...
The Issue: Panasonic has issued a Mandatory Product Safety Notice, indicating a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS-7 Recalled by Konica Minolta Medical Imaging USA, Inc. Due to Panasonic...
The Issue: Panasonic has issued a Mandatory Product Safety Notice, indicating a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...
The Issue: The firm will be updating the Instructions for Use for the product. Current...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Observer SD Recalled by Zeiss, Carl Inc Due to In certain eyepiece...
The Issue: In certain eyepiece configurations the laser shutter may not close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)...
The Issue: The firm will be updating the Instructions for Use for the product. Current...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed HARMONIC Ace¿ +7 Recalled by Stryker Sustainability Solutions...
The Issue: Stryker Sustainability Solutions has received an increase in reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivo 65 Recalled by Human Design Medical Llc Due to Some Vivo 65 devices...
The Issue: Some Vivo 65 devices have an unreleased version of the Firmware upgrade tool.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MX-10 surveillance laser system Product Usage: The expected usage of...
The Issue: Product has a nominal ocular hazard distance (NOHD) that is longer than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piperacillin and Tazobactam for Injection Recalled by Apotex Inc. Due to...
The Issue: Subpotent Drug: High Levels of Impurities Resulting in Decrease Potency
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Piperacillin and Tazobactam for Injection Recalled by Apotex Inc. Due to...
The Issue: Subpotent Drug: High Levels of Impurities Resulting in Decrease Potency
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.