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 25201–25220 of 48,770 recalls
Recalled Item: NxStage Express Fluid Warmer (FW-300 Recalled by NxStage Medical, Inc. Due...
The Issue: There is a potential risk of electrical fire when fluid leaks into the power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nokia BPM+ Wireless Blood Pressure Monitor Product System Recalled by...
The Issue: Device could not meet the requirements for systolic pressure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centron Product Usage: Vascular Recalled by Philips Healthcare Due to The...
The Issue: The first time an operator selects a new procedure type during a single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monsel's Solution (Ferric Subsulfate) Recalled by BioDiagnostic...
The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ESTRADIOL 20mg PELLET Recalled by Qualgen, LLC Due to Labeling: Incorrect or...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irinotecan Hydrochloride Injection Recalled by Ingenus Pharmaceuticals Llc...
The Issue: Superpotent Drug: High out of specification assay value results for potency.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irinotecan Hydrochloride Injection Recalled by Ingenus Pharmaceuticals Llc...
The Issue: Superpotent Drug: High out of specification assay value results for potency.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TESTOSTERONE 200 mg PELLET Recalled by Qualgen, LLC Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRSASelect II Recalled by Bio-Rad Laboratories, Inc Due to Abnormal...
The Issue: Abnormal coloration of agar plates and the growth of non-characteristic MRSA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRSASelect Recalled by Bio-Rad Laboratories, Inc Due to Abnormal coloration...
The Issue: Abnormal coloration of agar plates and the growth of non-characteristic MRSA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TR Toppers Brand Chopped Chocolate Pretzel Pieces. Item number B160-075...
The Issue: Recalling TR Toppers Brand Chopped Chocolate Pretzel Pieces due to the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...
The Issue: The latest on-site software version may not have been reinstalled at some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.