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. 2,450 recalls have been distributed to Maine in the last 12 months.
Showing 18641–18660 of 48,770 recalls
Recalled Item: Infinix-8000V with Catheterization Table CAT-850B or CAT-860B - Product...
The Issue: Bolts holding the longitudinal movement of catheterization tables may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinix-8000C with Catheterization Table CAT-850B or CAT-860B - Product...
The Issue: Bolts holding the longitudinal movement of catheterization tables may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 4000e Thyroid Uptake System Recalled by Capintec Inc Due to It is...
The Issue: It is possible that the collimators have screw hole locations that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbidopa and Levodopa Tablets Recalled by Mayne Pharma Inc Due to Product...
The Issue: Product Mix-Up: A foreign tablet was found in bottle.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ReStructure VANILLA PROTEIN POWDER NET WT. 527G POUCH & 27G Recalled by New...
The Issue: The firm was notified that the labeling does not include the word milk on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Merits E604 Pilot Navigator Stairlift - Product Usage: To transport Recalled...
The Issue: Pinion gear may disengage from track allowing lift to slip or jolt.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReWalk Personal 6.0 Recalled by Argo Medical Technologies Ltd Due to ReWalk...
The Issue: ReWalk Robotics received two complaints (one in the US; one in the Germany),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Lumbar Puncture Tray. Anesthesia Conduction Kit. 4826PL-20 - Product...
The Issue: Cases of Portex¿ Lumbar Puncture Tray Child, SKU #4826PL-20 had been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quetiapine Fumarate Extended-Release Tablets Recalled by The Harvard Drug...
The Issue: Labeling; Incorrect or Missing Package Insert: Product was packaged with the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quetiapine Fumarate Extended-Release Tablets Recalled by The Harvard Drug...
The Issue: Labeling; Incorrect or Missing Package Insert: Product was packaged with the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quetiapine Fumarate Extended-Release Tablets Recalled by The Harvard Drug...
The Issue: Labeling; Incorrect or Missing Package Insert: Product was packaged with the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quetiapine Fumarate Extended-Release Tablets Recalled by The Harvard Drug...
The Issue: Labeling; Incorrect or Missing Package Insert: Product was packaged with the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Elelyso (taliglucerase alfa) for injection Recalled by Pfizer Inc. Due to...
The Issue: Lack of Assurance of Sterility--Reports of loose metal ferrule crimps on...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: uDR 596i Digital Medical X-Ray Imaging System - Product Usage: Recalled by...
The Issue: Two issues were identified with the stationary x-ray system. 1. Some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Editing an assay Test Definition and switching to another assay s Test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4x4 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.