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. 1,023 recalls have been distributed to Vermont in the last 12 months.
Showing 14561–14580 of 47,027 recalls
Recalled Item: ETEST IMIPENEM RELEBACTAM. in vitro diagnostic Recalled by Biomerieux Inc...
The Issue: Major errors (Resistant result instead of Susceptible result) were observed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to There is the potential...
The Issue: There is the potential bacterial including Nontuberculous mycobacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooked Recalled by Avanti Frozen Foods Due to Potential Salmonella Contamination
The Issue: Potential contamination with Salmonella in frozen cooked shrimp
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TJM6008 Jamshidi" Crown Bone Marrow Biopsy/Aspiration Needle with Marrow...
The Issue: Due to complaints received regarding incomplete/open packaging seals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EJM4011 Jamshidi Evolve" Bone Marrow Biopsy/Aspiration Needle with Specimen...
The Issue: Due to complaints received regarding incomplete/open packaging seals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Sonicision Reusable Generator-converts electrical power from the...
The Issue: Potential for a manufacturing assembly error-may result in a non-functional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIN3018 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 18G x...
The Issue: Due to complaints received regarding incomplete/open packaging seals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kaluza C Flow Cytometry Software Versions: 1.0* Recalled by Beckman Coulter,...
The Issue: Software anomalies that may lead to the generation of erroneous results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA software. Used to manage microbiology test workflow from the Recalled...
The Issue: Software anomaly - Under certain conditions, unwanted alterations to results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)) Recalled by HOYU(US) LOGISTICS...
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Erythromycin Topical Solution USP Recalled by Teligent Pharma, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Erythromycin Topical Gel Recalled by Teligent Pharma, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prairie Wolf Distillery Alcohol Antiseptic 80% Recalled by Prairie Wolf...
The Issue: Hand sanitizer packaged in bottles that resemble beverage containers.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NEO DELTA SELFSAFE PUR T Recalled by Delta Med SpA Due to Problems related...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Configura Advance Chair Recalled by Accora Inc Due to The firm has...
The Issue: The firm has identified a potential for the backrest to become detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELTAVEN FASTFLASH Recalled by Delta Med SpA Due to Problems related to the...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELTAVEN Y Recalled by Delta Med SpA Due to Problems related to the...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA Self Safe 1 Recalled by Delta Med SpA Due to Problems related to...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELTAVEN Safety I.V. Catheter in Pur with closed system: a) Recalled by...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA SELFSAFE PUR 1 Recalled by Delta Med SpA Due to Problems related...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.