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. 2,455 recalls have been distributed to Maine in the last 12 months.
Showing 15921–15940 of 27,655 recalls
Recalled Item: Travel Kit Recalled by Madison Polymeric Engineering Due to The products...
The Issue: The products exhibit an unpleasant odor due to microbial contamination with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Step Endoscopic Cleaning Pad Recalled by Madison Polymeric Engineering...
The Issue: The products exhibit an unpleasant odor due to microbial contamination with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First aid/emergency kits containing Honeywell eyewash: CSM kit number...
The Issue: Firm is recalling first aid/emergency kits and cabinets which contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Push Button Blood Collection Set 0.8 x 19 Recalled by Becton...
The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Push Button Blood Collection Set 0.6 x 19 Recalled by Becton...
The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Ultra TouchTM Push Button Blood Collection Set 0.6 Recalled...
The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stem Extractor f/Guide Bar Recalled by Synthes, Inc. Due to There is a...
The Issue: There is a potential for the connection screw of the stem extractor to break.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nobel Biocare 17¿ Multi-Unit Abutment Recalled by Nobel Biocare Usa Llc Due...
The Issue: The product label has missing information, such as the lot number and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACS-NT Recalled by Philips Electronics North America Corporation Due to...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T5-NT Recalled by Philips Electronics North America Corporation Due to...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Lunar: a) DPX NT Recalled by GE Medical Systems Ultrasound &...
The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T: 1) Nova (Dual) Recalled by Philips Electronics North America...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiva systems Recalled by Philips Electronics North America Corporation...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiva systems Recalled by Philips Electronics North America Corporation...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T CX Recalled by Philips Electronics North America Corporation...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Lunar: a) DPX Duo Recalled by GE Medical Systems Ultrasound &...
The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T5 Model 78104 Product Usage: Indicated for use as a Recalled by Philips...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.0T Recalled by Philips Electronics North America Corporation Due to...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T10-NT Recalled by Philips Electronics North America Corporation Due to...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns TCM Recalled by Terumo Cardiovascular Systems Corporation Due to...
The Issue: Update to cooler-heater cleaning instructions.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.