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 47541–47560 of 48,770 recalls
Recalled Item: Carboplatin Injection Recalled by Hospira Inc. Due to Failed PH...
The Issue: Failed PH specification: The lots of Carboplatin Injection were manufactured...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nexium (esomeprazole magnesium) Delayed-Release Capsules Recalled by ASTRA...
The Issue: Adulterated Presence of Foreign Tablets/Capsules: Some bottles may contain a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Merge HEMO software. Recalled by Merge Healthcare, Inc. Due to The...
The Issue: The International Normalized Ratio (INR) value displayed in the study report...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVICEL Fibrin Sealant (Human) Rx Only. Manufacturer: Omrix...
The Issue: Ethicon and Omrix Biopharmaceuticals have received reports of air or gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KY LIQUIBEADS Vaginal Moisturizer Recalled by Mc-NEIL-PPC, Inc. Due to...
The Issue: Johnson & Johnson Healthcare Products (JJHP) is voluntarily recalling this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3mL 9NC Coagulation Sodium Citrate 3.2% Recalled by Greiner Bio-One North...
The Issue: Part of the lot received a lower concentration of citrate solution which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPIDER Surgical Instrument: Flexible Clip Applier The SPIDER¿ Surgical...
The Issue: Some clip applier units may be inadequate to achieve clip closure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian brand Varian ARIA Oncology Information System Recalled by Varian...
The Issue: A software anomaly has been identified with the Import Export Application...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bella Blanket Protective Coverlet Recalled by Beekley Corporation Due to...
The Issue: Imaging artifact can occur on mammogram result
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Brilliance 6 Recalled by Philips Medical Systems (Cleveland) Inc Due...
The Issue: Philips Healthcare was notified that several of the sixteen bolts securing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drager PT 4000 Phototherapy System Recalled by Draeger Medical Systems, Inc....
The Issue: A routine internal quality check found that the Drager PT 4000 Phototherapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mercaptopurine Tablets Recalled by Prometheus Laboratories Inc. Due to...
The Issue: Failed USP Dissolution Test Requirements: The recalled lots do not meet the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Earth's Best Organic Wheat Teething Biscuits Recalled by Lovin Oven, LLC Due...
The Issue: Earth's Best is recalling Earth's Best Organic Wheat Teething Biscuits...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Designer Whey Chocolate Recalled by Designer Protein LLC Due to The recall...
The Issue: The recall was initiated because Designer Protein has confirmed that...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Designer Whey Strawberry Recalled by Designer Protein LLC Due to The recall...
The Issue: The recall was initiated because Designer Protein has confirmed that...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Designer Whey French Vanilla Recalled by Designer Protein LLC Due to The...
The Issue: The recall was initiated because Designer Protein has confirmed that...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BD FACS 7-color Setup beads BD Biosciences Recalled by BD Biosciences,...
The Issue: Incorrect version of the CD was included with BD FACS 7 Color Setup Beads.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Foley procedural trays packaged in breather bags. The product Recalled...
The Issue: Incomplete seal on sterile packages of product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module model 8100. Subsequent product code: FPA The Recalled by...
The Issue: The recall was initiated because Carefusion identified a potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chorus Mobile Patient Lifter Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...
The Issue: ArjoHuntleigh has received a limited number of customer reports concerning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.