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. 2,379 recalls have been distributed to Maine in the last 12 months.
Showing 21501–21520 of 27,655 recalls
Recalled Item: Sureflex 200 Lithotripsy Fiber Recalled by American Medical Systems...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fiber Cleaver Recalled by American Medical Systems Innovation Center -...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sureflex 365 Lithotripsy Fiber Recalled by American Medical Systems...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sureflex 150 Lithotripsy Fiber Recalled by American Medical Systems...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stripper Recalled by American Medical Systems Innovation Center - Silicon...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sureflex 273 Lithotripsy Fiber Recalled by American Medical Systems...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reamer / Irrigator / Aspirator (RIA): RIA Drive Shafts Recalled by Synthes,...
The Issue: It was reported that the RIA Drive Shaft, Tube Assembly, and Reamer Head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPICC SOLO2 Catheter 4F Maximal Barrier Tray with Microintroducer...
The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPICC SOLO Catheter with Tip Location System (TLS) Stylet 4F Recalled by...
The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPICC SOLO Catheter with Sherlock 3CG (TPS) Stylet 5F Maximal Recalled...
The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Camino Intracranial Pressure Monitoring Catheter with Licox IMC Bolt...
The Issue: Integra LifeSciences is recalling the Camino Intracranial Pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPICC SOLO Catheter with Sherlock 3CG TPS Stylet 4F Maximal Recalled by...
The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allofix Insertion Kit Recalled by Musculoskeletal Transplant Foundation,...
The Issue: Musculoskeletal Transplant Foundation is recalling a certain lot of Allofix...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 6.5 mm Titanium Recon Screws w/T25 Stardrive (70mm Recalled by...
The Issue: certain lots of the Titanium Recon Screws (6.5mm ) were found to contain the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD¿- Solis Ambulatory Infusion Pump Recalled by Smiths Medical ASD, Inc....
The Issue: Smiths Medical has become aware of an issue with an intermittent occurrence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch & Lomb SoFlex SE Foldable intraocular Lens Product Usage: Recalled by...
The Issue: Haptics breaking during lens loading and insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch & Lomb SofPort Advanced Optics Aspheric Lens Recalled by Bausch &...
The Issue: Haptics breaking during lens loading and insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/ zeego systems Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: There exists a possible position sensor fault in the swivel base axis not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Science & Engineering Inc Recalled by American Science &...
The Issue: During factory testing, we discovered that Gemini systems could, in rare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0702-001-350Q Recalled by Stryker Instruments Div. of Stryker Corporation...
The Issue: Stryker Instruments is initiating a recall of the Neptune 2 Waste Management...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.