Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,046 recalls have been distributed to Wyoming in the last 12 months.
Showing 12061–12080 of 48,219 recalls
Recalled Item: Dark Raspberry Classic. Net wt. 1.4 oz. . Recalled by Queen Bee Gardens, LLC...
The Issue: Products may potentially contain one or more of the following undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fudge Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 Recalled by Queen...
The Issue: Products may potentially contain one or more of the following undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Honey Caramels Huckleberry. Net wt. 5.87 oz. PLU Code: 788394 Recalled by...
The Issue: Products may potentially contain one or more of the following undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Honey Caramels Vanilla. PLU Code: 788394 12332 0 Product available Recalled...
The Issue: Products may potentially contain one or more of the following undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Centricity PACS RA1000 Recalled by GE Healthcare, LLC Due to Potential for...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Enterprise Web Recalled by GE Healthcare, LLC Due to Potential...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FIRMap" Catheter Recalled by Abbott Due to Incorrect product labeling.
The Issue: Incorrect product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Cardiology CA1000 Recalled by GE Healthcare, LLC Due to Potential...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Radiology RA600 Recalled by GE Healthcare, LLC Due to Potential...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer Zero Footprint Client Recalled by GE Healthcare,...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GaviLyte -C (Polyethylene Glycol 3350 Recalled by Lupin Pharmaceuticals Inc....
The Issue: Failed Stability Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TEG 5000 Functional Fibrinogen Reagent Recalled by Haemonetics Corporation...
The Issue: Due to a shift in the citrated blood range for a normal population, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Wet -Field Eraser Recalled by Beaver Visitec International, Inc. Due to...
The Issue: Boxes labeled as Wet-Field Eraser, 18GA Blunt Tip, 45Deg., were shipped...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1 Series CX phototherapy units equipped with Daavlin's ClearLink Control...
The Issue: Software issue, resuming an interrupted treatment will result in swap of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4 Series CX phototherapy units equipped with Daavlin's ClearLink Control...
The Issue: Software issue, resuming an interrupted treatment will result in swap of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-Line ventilator adaptor Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential of reduced oxygenation or pneumothorax/barotrauma to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-Line ventilator adaptor Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential of reduced oxygenation or pneumothorax/barotrauma to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Field replacement back up batteries distributed on or after April 1 Recalled...
The Issue: Backup batteries can fail earlier than their estimated life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioTek EP-TRACER Software V2.x. Recalled by CardioTek BV Due to Device...
The Issue: Device did not pass electrical safety testing for adequate insulation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Back up batteries in Avance CS2 and Avance CS2 Pro Recalled by GE...
The Issue: Backup batteries can fail earlier than their estimated life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.