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. 2,542 recalls have been distributed to Maine in the last 12 months.
Showing 4581–4600 of 27,655 recalls
Recalled Item: EndoVive 20Fr Push Standard PEG Kit w/ENFit (Box 2)-Indicated for Recalled...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20Fr Push Safety PEG Kit (Box 2)-Indicated for enteral Recalled by...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20 Fr Safety PEG Push w/ENFit Kit (Box 2)-Indicated Recalled by...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20Fr Push Standard PEG Kit (Box 2)-Indicated for enteral Recalled...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate 3 Left Ventricular Assist System (LVAS): 1. HeartMate 3 Recalled...
The Issue: Observed outflow graft deformation known as Extrinsic Outflow Graft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate II Left Ventricular Assist System (LVAS): 1. HeartMate II Recalled...
The Issue: Observed outflow graft deformation known as Extrinsic Outflow Graft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convatec EsteemBody Soft Convex Recalled by ConvaTec, Inc Due to Convatec...
The Issue: Convatec Inc is conducting a Voluntary Medical Device Recall (removal) for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Single Use Electrosurgical Knife Product Name: Olympus Single...
The Issue: A deterioration of the cutting knife, including overheating and burning, can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Single Use Electrosurgical Knife KD-645 Product Name: Olympus...
The Issue: A deterioration of the cutting knife, including overheating and burning, can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Origio Sperm Wash Medium Pack of Ten 10ml bottles - Recalled by...
The Issue: Low concentration of sodium pyruvate in the wash could compromise gamete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Origio Sperm Wash Medium Pack of Five 60ml bottles - Recalled by...
The Issue: Low concentration of sodium pyruvate in the wash could compromise gamete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Origio Sperm Wash Medium Pack of Five 60ml bottles - Recalled by...
The Issue: Low concentration of sodium pyruvate in the wash could compromise gamete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivance Neonatal ArcticGel Pads Recalled by Medivance Inc. Due to Neonatal...
The Issue: Neonatal pads are experiencing reduced water flow, which may reduce or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARTO VIZIGO Bi-Directional Guiding Sheath Recalled by Biosense Webster,...
The Issue: Due to a manufacturing issue, device under process validation phase were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abre Venous Self-expanding Stent System Recalled by Medtronic Inc. Due to...
The Issue: There is a potential for sterile package breach.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-Rad Recalled by Bio-Rad Laboratories Due to Due to incorrect...
The Issue: Due to incorrect calibrations and controls, their is a potential of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...
The Issue: Their is a potential that Oximeter may automatically power off and on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...
The Issue: Their is a potential that Oximeter may automatically power off and on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIVA 24 Inch Widescreen LCD Touch Display - Used with Recalled by Philips...
The Issue: If the DIVA touch display generates touch inputs without user interaction,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...
The Issue: Their is a potential that Oximeter may automatically power off and on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.