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. 2,244 recalls have been distributed to Vermont in the last 12 months.
Showing 43821–43840 of 47,027 recalls
Recalled Item: Medi-Trace Cadence Adult Radiotransparent Defibrillation Electrode Product...
The Issue: Defibrillation Electrodes may arc/spark result in thermal damage to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glenmark Gabapentin Tablets Recalled by Glenmark Generics Inc., USA Due to...
The Issue: Chemical Contamination: Gabapentin Sodium tablets is recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glenmark Pravastatin Sodium Tablets Recalled by Glenmark Generics Inc., USA...
The Issue: Chemical Contamination: Pravastatin Sodium Tablets isbeing recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glenmark Topiramate Tablets Recalled by Glenmark Generics Inc., USA Due to...
The Issue: Chemical Contamination: Topiramate Tablets is being recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROFILE-V MEDTOXScan Drugs of Abuse Test System. For the rapid Recalled by...
The Issue: Review of validation information and customer complaints which indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rite Aid brand Maximum Strength Tussin Cough & Cold Mucus Relief CF Recalled...
The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: remel RapID Yeast Plus System Recalled by Remel Inc Due to Mislabeling
The Issue: The two reagents supplied in the RapID Yeast Plus System kit (Reagent A and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20mm addEASE(TM) Binary Connector with 17 Ga. Needle for use Recalled by B....
The Issue: Possible solution leakage at the interface of the addEASE(TM) Binary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13mm addEASE(TM) Binary Connector with 17 Ga. Needle for use Recalled by B....
The Issue: Possible solution leakage at the interface of the addEASE(TM) Binary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPC Fine Mesh Cassette for the Leica LPC Printer. Part No: 14060546848...
The Issue: An LPC Fine Mesh Cassette failed to stay closed during processing operations.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTS PANELS Recalled by Polymer Technology Systems, Inc. Due to Internal...
The Issue: Internal investigation demonstrated under-recovery for glucose when tested...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas¿ 8000 modular analyzer series software version 03-01 Recalled by Roche...
The Issue: When using the cobas e 602 module, Diluent Multiassay may be used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExoShape Soft Tissue Fastener 12 mm x 30 mm by Medshape Solutions, INC. Due...
The Issue: Expiration date on the patient label and date on the product carton were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software correction applies to customers who use the RT Therapist Recalled...
The Issue: Software update to fix multiple safety related issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxcarbazepine Oral Suspension Recalled by Boehringer Ingelheim Roxane Inc...
The Issue: Resuspension Problems: Recalled lot did not meet resuspendability requirements.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TOSHIBA Kalare Diagnostic X-Ray System K110785 Recalled by Toshiba American...
The Issue: Firm initiated recall because when radiographic conditions with the small...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products CK-MB Calibrators Recalled by...
The Issue: Internal testing demonstrated that opened-reconstituted VITROS CK-MB...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.