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. 1,712 recalls have been distributed to Vermont in the last 12 months.
Showing 40501–40520 of 47,027 recalls
Recalled Item: High Mowing Organic Sprouting Seeds Ancient Eastern Blend Recalled by High...
The Issue: Contains undeclared wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Popsicle Orange Cherry Grape 20 pops Net 33 fl oz Unilever Englewood Cliffs...
The Issue: Unilever United States, Inc. is voluntarily recalling a limited number of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medtronic Recalled by Medtronic Neuromodulation Due to Medtronic...
The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPort Slim Implantable Port Recalled by Bard Access Systems Due to...
The Issue: Labeling discrepancy.The label states that the implantable port contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-10" Hemoglobin Testing System Recalled by Bio-Rad Laboratories, Inc. Due...
The Issue: On a rare occasion the D-10 software might generate an extra result by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Activa RC (37612) Recalled by Medtronic Neuromodulation Due to...
The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic neurostimulators. Restore (37711) Recalled by Medtronic...
The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part 475620 Intramedullary Bone Saw CAM Assembly Size 12mm Recalled by...
The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw.The Saw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part 475625 Recalled by Biomet, Inc. Due to Incorrect labeling on specific...
The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw. The Saw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novocastra Liquid Mouse Monoclonal Antibody Glutathione S-Transferase pi...
The Issue: Novocastra Liquid Mouse Monoclonal Antibody Glutathione S-Transferase pi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part 475630 Recalled by Biomet, Inc. Due to Incorrect labeling on specific...
The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw. The Saw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advil PM Caplets Recalled by Pfizer Us Pharmaceutical Group Due to Subpotent...
The Issue: Subpotent Drug: This lot is being recalled because of out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Natural-Knee¿ II Constrained Knee System NKII CCK TIB INS SZ00/0-L Recalled...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ N-K II DOMED ALL-POLY PAT Recalled by Zimmer, Inc. Due to A...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ II Posterior Stabilized (P.S.) Condylar Tibial Inserts: N-K II...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo" Knee System: APOLLO PATELLA SZ0 28MM R Recalled by Zimmer, Inc. Due...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo" Knee System: PS TIB INS SZ0/16MM APOLL PS TIB Recalled by Zimmer,...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ Congruent Tibial Insert with Screw: SF-CON TIB INS LT Recalled...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ II System ULTRA CONG INS LT SZA/9MM ULTRA CONG Recalled by...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gender Solutions" Natural-Knee¿ Flex System: N-K FLEX MBACK SZ 0 Recalled by...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.