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. 1,059 recalls have been distributed to Maine in the last 12 months.
Showing 14161–14180 of 48,770 recalls
Recalled Item: ADVIA Centaur SARS-CoV-2 Antigen Assay (100 Test Kit) Recalled by Siemens...
The Issue: Data provided in the Emergency Use Authorization (EUA) submission was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS Clostridium Difficile Toxin A&B Recalled by bioMerieux, Inc. Due to...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS B.R.A.H.M.S. PROCALCITONIN PCT Recalled by bioMerieux, Inc. Due to...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Recalled by Philips Healthcare Due to The Aleva monitor...
The Issue: The Aleva monitor requires certain labels to be applied, some of which are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuikClot Combat Gauze-For Temporary External Use To Control Traumatic...
The Issue: Lack of Packaging seal integrity may result in a sterile barrier breach.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS RUB IgG (RBG) Recalled by bioMerieux, Inc. Due to bioMerieux has been...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS Lyme IgM II (LYM) Recalled by bioMerieux, Inc. Due to bioMerieux has...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS LH Recalled by bioMerieux, Inc. Due to bioMerieux has been receiving...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS SARS-COV-2 IgM Recalled by bioMerieux, Inc. Due to bioMerieux has been...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM SARS-CoV-2 Antigen Assay (100 Test Kit) Recalled by Siemens...
The Issue: Data provided in the Emergency Use Authorization (EUA) submission was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA One 3.1 Brain application The device is intended for Recalled by...
The Issue: The firm has become aware of a software anomaly affecting ROSA One 3.1 Brain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate Testosterone Propionate Recalled by New Vitalis...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 55/14 (fluticasone propionate 55 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Phenylbutyrate Powder Recalled by SigmaPharm Laboratories LLC Due to...
The Issue: Failed Impurities/Degradation Specifications; Out of Specification impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardiosave Li-Ion Battery Pack Recalled by Datascope Corp. Due to A...
The Issue: A Cardiosave Lithium-Ion Battery Pack used during protocol testing failed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The da Vinci Xi and X surgical systems (IS4000 and Recalled by Intuitive...
The Issue: Incorrect expiration date on its package labeling (shipper box and inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.