Product Recalls in Vermont
Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,343 recalls have been distributed to Vermont in the last 12 months.
Showing 22861–22880 of 47,027 recalls
Recalled Item: AF w/AS 550 x 1-14ML/HR 5ML-60LO CPNB 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: AF550x5ML/H 2ML 60LO 6" DUAL CATHS Recalled by Arrow International Inc Due...
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: AF 550 x 5ML/HR 2ML 60LO CPNB Recalled by Arrow International Inc Due to...
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: AF 550 x 5ML/HR CPNB Recalled by Arrow International Inc Due to Possible...
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: AF 550 x 5ML/H FH DL 30hole SAT C Recalled by Arrow International Inc Due to...
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: AF 550x8ML/H 2ML 15LO 8.7" DUAL CATHS 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: 0F 550 x 8ML/HR 2ML 60LO CPNB Recalled by Arrow International Inc Due to...
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: 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: AF w/AS 550x 0.5 7 ml/hr Recalled by Arrow International Inc Due to Possible...
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: AF550x5ML/H 2ML 60LO 6" CATH Recalled by Arrow International Inc Due to...
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: Pantoprazole Sodium Delayed-Release Tablets Recalled by Jubilant Cadista...
The Issue: Discoloration: Presence of dark discoloration or brown spots on the edges of...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: 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: 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: P28 Recalled by Paragon 28, Inc. Due to Mislabeling
The Issue: It has been determined that the wedge implant kit is permanently mislabeled...
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: 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: 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.