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. 2,250 recalls have been distributed to Vermont in the last 12 months.
Showing 41501–41520 of 47,027 recalls
Recalled Item: ALTRUS¿ THERMAL TISSUE FUSION Recalled by ConMed Corporation Due to The...
The Issue: The affected lots were exposed to a higher than acceptable level of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zeiss brand IOLMaster 500 Recalled by Carl Zeiss Meditec, Inc. Due to The...
The Issue: The user database delivered for download contained an erroneous value....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zeiss brand IOLMaster Recalled by Carl Zeiss Meditec, Inc. Due to The user...
The Issue: The user database delivered for download contained an erroneous value....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALTRUS¿ THERMAL TISSUE FUSION Recalled by ConMed Corporation Due to The...
The Issue: The affected lots were exposed to a higher than acceptable level of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model FL14E Rose BedsThe Rose Bed is an AC-powered adjustable Recalled by...
The Issue: It was reported that the siderail may appear latched when it is not, due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tacrolimus Capsules Recalled by Sandoz Incorporated Due to Cross...
The Issue: Cross Contamination with Other Products: findings of carryover of trace...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Human Chorionic Gonadotropin Recalled by Medisca Inc. Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength; Firm states that erroneous...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SuperDigestZyme (Z22) Recalled by Apex Energetics Due to Apex Energetics is...
The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RepairVite (K63) Recalled by Apex Energetics Due to Apex Energetics is...
The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GlutenFlam (K-52) Enzyme & Bioflavonoid Dietary Supplement Recalled by Apex...
The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: LGS-Zyme (Z12) Recalled by Apex Energetics Due to Apex Energetics is...
The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: THUNDER¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COUGAR¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProVia¿ CROSSING GUIDEWIRE Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZINGER¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTAIN HYBRID¿ Guide Wire Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THUNDER¿ Extra Support Guidewire Recalled by Medtronic Vascular Due to...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zinger¿ Stainless Steel Workhorse Guidewire Recalled by Medtronic Vascular...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ Recalled by...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Applied Medical's Inzii¿ 12/15mm Retrieval System. Applieds Inzii Tissue...
The Issue: Applied Medical is conducting a voluntary recall of the Inzii¿ 12/15mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.