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. 2,518 recalls have been distributed to Maine in the last 12 months.
Showing 10721–10740 of 48,770 recalls
Recalled Item: NEO-fit Neonatal Endotracheal Tube Grip Recalled by CooperSurgical, Inc. Due...
The Issue: Firm has received 11 complaints involving a loose or detached metal clips,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Susvimo (ranibizumab injection) Recalled by Genentech Inc Due to Defective...
The Issue: Defective Delivery System: Commercial implants do not meet the filed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg Recalled by SUN...
The Issue: Presence of Foreign Substance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GFUEL brand Watermelon Limeade Energy Drink Recalled by G FUEL LLC Due to...
The Issue: Product label does not declare the correct amount of caffeine.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Atrium Ocean Wet Suction Water Seal Chest Drain- Product Code: 2002-000...
The Issue: Warehouse experienced temperature excursions in July and August 2021. It was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom Progressa Bed System Recalled by Baxter Healthcare Corporation Due...
The Issue: The compression links on impacted Progressa beds, listed in Appendix A, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerate PhenoTest BC kit Recalled by Accelerate Diagnostics Inc Due to...
The Issue: Due improperly formulated and released bulk lot of fluorescence in situ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerate PhenoTest BC kit Recalled by Accelerate Diagnostics Inc Due to...
The Issue: Due improperly formulated and released bulk lot of fluorescence in situ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS3 Iridium - Visionsense Infrared (IR) Fluorescence Miniature Microscope...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS3 Iridium Visionsense Infrared (IR) Fluorescence Light Integrator (Beam...
The Issue: Broken Optical fiber cable damage can occur through handling or bending and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS3 Iridium Visionsense Infrared (IR) Fluorescence Miniature Microscope...
The Issue: Broken Optical fiber cable damage can occur through handling or bending and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 18239: ASM Omnipod Dash PDM Recalled by Insulet Corporation Due to The firm...
The Issue: The firm has become aware of PDM battery issues, including battery swelling,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GI4000 Electrosurgical Unit - intended to deliver electrosurgical outputs to...
The Issue: Two electronic diode components (D1 & D4) placed in the reverse orientation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extension Tabletop for Operating Table System 1140 Recalled by Getinge Usa...
The Issue: The back rest may unintentionally drop suddenly, resulting in adverse health...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visualase Cooled Laser Applicator System (VCLAS) 9735560 .4MM CORE FIBER...
The Issue: Due to a defect in the outer pouch sterile seal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GentleWave System APM Procedure Instrument with Matrix Recalled by Sonendo...
The Issue: Procedure Instruments with erroneous unit carton labels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GentleWave System Posterior CleanFlow Procedure Instrument with Matrices...
The Issue: Procedure Instruments with erroneous unit carton labels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Laser System Recalled by Spectranetics Corporation Due to Laser...
The Issue: Laser System may detect Error 106 or Error 108 System Failures that will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine Hydrochloride Jelly USP Recalled by Akorn, Inc. Due to CGMP...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tobramycin Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP Deviations:
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.