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. 2,460 recalls have been distributed to Maine in the last 12 months.
Showing 14601–14620 of 27,655 recalls
Recalled Item: AF 550 x 8ML/HR 2ML 15LO CPNBMT8015XL CP Recalled by Arrow International Inc...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YXLON Cougar Cabinet X-Ray System Product Usage: The products are Recalled...
The Issue: Failure to meet the requirement of the performance standard for cabinet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YXLON Cheetah cabinet X-Ray System Product Usage: The products are Recalled...
The Issue: Failure to meet the requirement of the performance standard for cabinet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C3 Wave App Recalled by Medical Components, Inc dba MedComp Due to When the...
The Issue: When the iPad is updated with Apple iOS software version 12, the C3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Peg Guide Extender Recalled by TriMed Inc. Due to The spring on the...
The Issue: The spring on the PEG-Extender can rust due to the type of steel used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Wrist Hook Dorsal Impactor Recalled by TriMed Inc. Due to The WHD/WHV...
The Issue: The WHD/WHV impactors can rust over time due to an improper manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Hex Driver 1.2 Recalled by TriMed Inc. Due to The epoxy on Apex...
The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Countersink 1.7mm Recalled by TriMed Inc. Due to The epoxy on Apex...
The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Locking Drill Guide Recalled by TriMed Inc. Due to The epoxy on Apex...
The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-2000 Analyzer Recalled by Tosoh Bioscience Inc Due to There is a...
The Issue: There is a possibility that the liquid suction pump on some AIA-2000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Thermal Chamber Motor Cable located in the following models:...
The Issue: Thermal chamber motors have electrical cables with single insulation rather...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph Horizon a) 3R Recalled by Siemens Medical Solutions USA, Inc. Due...
The Issue: The terminals on the plug may become loose and overheat.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph mCT: a) S(64)-3R Recalled by Siemens Medical Solutions USA, Inc....
The Issue: The terminals on the plug may become loose and overheat.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-2000 Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience...
The Issue: Tosoh Bioscience has become aware of a potential issue with the AIA-900 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-900Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience has...
The Issue: Tosoh Bioscience has become aware of a potential issue with the AIA-900 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aisys Anesthesia System. Sold under the following product names: AISYS...
The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aisys CS2 Anesthesia System. Sold under the following product names: AISYS...
The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Touchscreen display kit. Sold under the following product names: TOUCHSCREEN...
The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Sample Handler Prime. In vitro diagnostic testing of clinical...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer: In vitro diagnostic testing of clinical Recalled...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.