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 47661–47680 of 48,770 recalls
Recalled Item: Equinoxe Reverse Glenosphere Locking Screw Intended for Primary and Reverse...
The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Anatomic Replicator Plate Intended for Primary and Reverse Total...
The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Reverse Compression Screw Intended for Primary and Reverse Total...
The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Reverse Shoulder Fracture Adapter Tray Screw Intended for Primary...
The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZEE Antiseptic Wipes Recalled by Dukal Corp. Due to Microbial contamination...
The Issue: Microbial contamination of Non Sterile Product; contamination with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dukal Corporation BZK Swab Recalled by Dukal Corp. Due to Microbial...
The Issue: Microbial contamination of Non Sterile Product; contamination with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kleenex Luxury Foam Hand Sanitizer Recalled by Kimberly-Clark Corporation...
The Issue: Microbial Contamination of Non-Sterile Products; The affected lots were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kleenex Foam Hand Sanitizer Recalled by Kimberly-Clark Corporation Due to...
The Issue: Microbial Contamination of Non-Sterile Products; The affected lots were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IQF Oysters 3lbs Recalled by KOREAN FARM, INC. Due to Korean Farm is...
The Issue: Korean Farm is recalling Assi Brand Korean Oysters because they have been...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The 2.7mm Drilling Guide is a reusable instrument used in Recalled by...
The Issue: Integra' s quality system noted an adverse trend in complaints for breakage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Xcelera Connect Recalled by Philips Healthcare Inc. Due to Xcelera...
The Issue: Xcelera Connect R2.1 L 1 SP2 , incomplete information arriving from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ocean Manna Korean IQF Oysters Recalled by Pacific Giant, Inc Due to Pacific...
The Issue: Pacific Giant is recalling all frozen (IQF) oyster meat and 1/2 shell...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...
The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...
The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: seprafilm¿ Procedure Pack ADHESION BARRIER Re-order Number: 5086-02 Product...
The Issue: Sterility of product may be compromised due to packaging defect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: seprafilm¿ Single Site ADHESION BARRIER Re-order Number: 6641-01 Product...
The Issue: Sterility of product may be compromised due to packaging defect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator Recalled by Maquet...
The Issue: It has come to firm's attention that, in some rare cases, the blood outlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream DRX-1 System Battery --- Made in U.S.A. for Carestream Health...
The Issue: Carestream DRX-1 System batteries manufactured before June 2012 due to two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware through complaints of a potential safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Concha Therm Neptune Humidifier Recalled by Teleflex Medical Due...
The Issue: Speaker Failure. If the speaker fails and an event occurs which would...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.