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. 2,317 recalls have been distributed to Maine in the last 12 months.
Showing 41441–41460 of 48,770 recalls
Recalled Item: Pristiq (desvenlafaxine) Extended-Release Tablets 50 mg Recalled by Pfizer...
The Issue: Presence of Foreign Tablets/Capsules: Pfizer is recalling 50 mg Pristiq...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tissue-Tek PARAFORM PROC/EMB/MEDIUM Recalled by Sakura Finetek USA Inc Due...
The Issue: This Lot has variations in melting temperature.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes Craniomaxillofacial Distraction System (AB Distractor Bodies...
The Issue: DePuy Synthes is initiating a recall of certain lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet PowerLED 700. Product Usage Recalled by Maquet Medical Systems USA...
The Issue: Maquet has identified an issue with the Maquet PowerLED 700 (certain serial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio2 PT/INR Professional Test Strips Recalled by Alere San Diego,...
The Issue: Test Strips may report an inaccurately low INR result. Several patients had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExacTrac 5.5 Recalled by Brainlab AG Due to When using a specific plan...
The Issue: When using a specific plan update workflow in combination with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant Nasal CPAP (continuous positive airway pressure) Prong Recalled by...
The Issue: The Infant Nasal CPAP Prong has the potential to detach from the Nasal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZPass Passer Recalled by Biomet, Inc. Due to The nitinol wire or...
The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZPass Suture Retriever Recalled by Biomet, Inc. Due to The nitinol wire or...
The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZPass Nylon Monofilament Single Pack Recalled by Biomet, Inc. Due to The...
The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Super ARTHGOLD 500mg Recalled by Sung Soo Kim Due to Undeclared Indomethacin
The Issue: Marketed Without an Approved NDA/ANDA; Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Children's Triacting Night Time Cold & Cough with PE (diphenhydramine...
The Issue: Presence of Precipitate: Small amounts of diphenydramine and mannitol...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ReTurn 7500/7500 Aid Recalled by Handicare USA, Inc. Due to During the...
The Issue: During the period of April 2009 May 2011, Handicare AB used a wing handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxandrolone Tablets Recalled by Upsher Smith Laboratories, Inc. Due to...
The Issue: Labeling: Missing Label; Three cases of product (total of 36 bottles) were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Day Time Cold & Flu Recalled by P&L Developments, LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: Phenylephrine component is subpotent.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HALOPERIDOL DECANOATE INJECTION Recalled by Fresenius Kabi USA LLC Due to...
The Issue: Failed Impurities/Degradation Specifications: Fresenius Kabi is recalling...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOSARTAN POTASSIUM Tablets Recalled by Golden State Medical Supply Inc. Due...
The Issue: Presence of Foreign Substance; some bottles may contain debris that was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Greens+ Vegan Crisp Bars - Dark Chocolate Peanut Butter in 1.4 oz packages....
The Issue: Undeclared milk protein in chocolate coating.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Greens+ Vegan Crisp Bars - Dark Chocolate Almond Coffee Crisp Recalled by...
The Issue: Undeclared milk protein in chocolate coating.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Organic traditions DARK CHOCOLATE SACHA INCHI SEEDS***DAIRY & SUGAR FREE...
The Issue: Undeclared milk allergen
Recommended Action: Do not consume. Return to store for a refund or discard.