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. 945 recalls have been distributed to Vermont in the last 12 months.
Showing 34281–34300 of 47,027 recalls
Recalled Item: EDTA Disodium Injectable Recalled by Downing Labs, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zinc Sulfate (Elemental) Injection Recalled by Downing Labs, LLC Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magnesium Sulfate 50% Injectable Recalled by Downing Labs, LLC Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magnesium Sulfate Injection (4060mOsm/L) Recalled by Downing Labs, LLC Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EDTA Calcium Disodium Injectable Recalled by Downing Labs, LLC Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Piracetam Injection Recalled by Downing Labs, LLC Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Myelo-Nate CSF Sampling Kit Recalled by Utah Medical Products, Inc Due to...
The Issue: Utah Medical is conducting a recall of Myelo-Nate CSF Sampling Kit due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIASTAT anti-Nuclear antibody (ANA) / DIASTAT ANA ELISA. Catalog Number:...
The Issue: Complaint investigation concluded that although product quality requirements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune Plus Recalled by TZ Medical Inc. Due to The IFU of the Neptune Plus...
The Issue: The IFU of the Neptune Plus Pads, does not match that submitted in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome" Chronic Catheter Kit Symmetrical Tip Recalled by Covidien LLC...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip 14.5 Fr/Ch (4.8mm)...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Electronics...
The Issue: The following MRx software issue has been identified: MRx model M3535A with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SSS Reprocessed Zimmer Recalled by Stryker Sustainability Solutions Due to...
The Issue: It was reported that packaging was not properly sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Taut Intraducers 10/BX7.5 FR 3.5 Recalled by Teleflex Medical Due to The...
The Issue: The defective component can cause gas leakage through the device. This can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Two-stage and three-stage I.V. poles are shipped as an optional Recalled by...
The Issue: It was identified by a customer complaint that some I.V. poles were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovoCut Suture Manager Recalled by Ceterix Orthopedics, Inc. Due to The...
The Issue: The NovoCut Suture Manager device may cut the suture during knot tensioning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access CEA Assay Recalled by Beckman Coulter Inc. Due to Beckman Coulter is...
The Issue: Beckman Coulter is recalling the Access CEA reagent packs because they were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.