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. 2,371 recalls have been distributed to Maine in the last 12 months.
Showing 22901–22920 of 27,655 recalls
Recalled Item: Equate Moisture Last Multi-Purpose Solution Recalled by Bausch & Lomb Inc-...
The Issue: Product lot did not meet the specification for its disinfectants at the time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Spirit Combo insulin infusion pump sold as part of Recalled by...
The Issue: The insulin pump may lose time and date settings during a power interruption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Joerns EasyCare Bed Product Usage: The AC-powered adjustable hospital bed...
The Issue: The Easy-Care Care-Lock feature installed at the foot of the bed may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery Elbow Humeral Trial Product Usage: Biomet manufactures a variety...
The Issue: An investigation identified that the product was incorrectly manufactured as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: siemens Dimension¿ Phenytoin Flex¿ Reagent Cartridge The PTN method used...
The Issue: Internal testing has confirmed a low absorbance range between the levels 1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Bone Level Implant 04.1 mm RC Recalled by Straumann USA, LLC Due...
The Issue: Product transfer piece was fitted with a Narrow Connect (NC) instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Switches used with the following systems: Philips Allura Xper Systems...
The Issue: Loss of key image functionality due to a bent pedal of the Footswitch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector...
The Issue: Loss of key image functionality due to a bent pedal of the Footswitch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare Perfecto 2 V Oxygen Concentrator The finished device is Recalled by...
The Issue: It was determined that a defective sieve bed subassembly enabled zeolite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zeego systems Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A cable inside the C-arm systems may have been routed in an inappropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digital Mobile X-ray Systems used to take diagnostic radiographic exposures...
The Issue: There is a potential for unintended and erratic motion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoswift PGCL [poly(glycolide-co-caprolactone)] Absorbable Surgical Suture...
The Issue: CP Medical Inc. is recalling five lots of Monoswift PGCL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE /IMMULITE 1000 Systems COR Cortisol Recalled by Siemens Healthcare...
The Issue: Customer complaints were received for positive bias reported on the controls...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: External power supply adaptors that accompany Clinitek Status Connect System...
The Issue: The external power supply for the Clintek Status analyzer, which is provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carescape Patient Data Module Recalled by GE Healthcare, LLC...
The Issue: GE Healthcare has recently become aware of a potential safety issue to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: External power supply adaptors that accompany Clinitek Status+ The Clinitek...
The Issue: The external power supply for the Clintek Status analyzer, which is provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: External power supply adaptors that accompany Clinitek Status Power Supply...
The Issue: The external power supply for the Clintek Status analyzer, which is provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoWrist Stapler 45 instrument for the da Vinci Si System Recalled by...
The Issue: Intuitive is issuing an urgent product notice to all users of the EndoWrist...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number:...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice¿ Multifunction Electrode Part Number: MC171 OH Recalled by...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.