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. 2,503 recalls have been distributed to Vermont in the last 12 months.
Showing 7761–7780 of 27,157 recalls
Recalled Item: POLIGRIP ADH CREAM FREE 2.4OZ Recalled by Family Dollar Stores, Llc. Due to...
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIQUICK PREGNANCY TEST 1CT Recalled by Family Dollar Stores, Llc. Due to...
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CURAD FIRST AID KIT Recalled by Family Dollar Stores, Llc. Due to Affected...
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIMPLY SALINE NASAL MIST 3.1 OZ Recalled by Family Dollar Stores, Llc. Due...
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FIXODENT ORG CREAM 2.4OZ Recalled by Family Dollar Stores, Llc. Due to...
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFESTYLES ULTRA SENSITIVE CONDOMS 12CT Recalled by Family Dollar Stores,...
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veriquick Pregnancy Test 2CT Recalled by Family Dollar Stores, Llc. Due to...
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GS DENTURE CLEANSER GRN TAB 40CT Recalled by Family Dollar Stores, Llc. Due...
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B L BIOTRU MULTI PURPOSE SOLUTION 4 FLOZ Recalled by Family Dollar Stores,...
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AT HOME MARIJUANA TEST STRIP Recalled by Family Dollar Stores, Llc. Due to...
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SKYN ORIGINAL NON LATEX CONDOM 12CT Recalled by Family Dollar Stores, Llc....
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEW SKIN LIQUID BANDAGE CLEAR .3FL OZ Recalled by Family Dollar Stores, Llc....
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) CVS Health Sterile Surgical Pads Recalled by ASO LLC Due to The product...
The Issue: The product falls apart during handling after removal from its primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The E-100 Generator (PN 374848-09) is a bipolar electrosurgical unit...
The Issue: Due to preventative maintenance (PM) not being performed on E-100 generators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revogene Recalled by Meridian Bioscience Inc Due to When a run is aborted,...
The Issue: When a run is aborted, the cooling period protection does not occur and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CereLink ICP Monitor Recalled by Integra LifeSciences Corp. Due to Integra...
The Issue: Integra has received complaints associated with ICP readings drifting to -50...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Cholesterol- For the quantitative in vitro determination of...
The Issue: Product fails to meet the performance claims quoted on the kit insert:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethemet cables are missing one or both ferrite cores therefore the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethemet cables are missing one or both ferrite cores therefore the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: etouchus Recalled by Touch US Llc Due to Device was marketed without FDA...
The Issue: Device was marketed without FDA 510(k) clearance or a PMA.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.