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. 1,680 recalls have been distributed to Wyoming in the last 12 months.
Showing 42721–42740 of 48,219 recalls
Recalled Item: HGP II ACETABULAR CUP BON Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERI SCR. 3.5MM X 10MM PERI SCR. 3.5MM X 12MM Recalled by Zimmer, Inc. Due...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREE-LOCK LAG SCREW Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONE-PIECE LAG SCREW 11MM. Item codes starting with 00225900. Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX II KEYLESS TUBE Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTERLOCKING IM SCREW 4.5 and INTERLOCKING IM SCREW LG Some Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6 DEGREE COCR FEM HEAD 36 Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Item codes starting with 001930 LAG SCR 12.7D X 55MM SHOR up to 155 MM...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MODULAR CUP NEUTRAL LINER MODULAR CUP 10 DEGREE LIN MODULAR Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FEM HD ION (various sizes) Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HERBERT MINI BONE SCREW 2 and HERBERT/WHIPPLE C ANN BONE. Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ITST ANTI-ROTATION SCREW and FEM IM NAIL (10MM Recalled by Zimmer, Inc. Due...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRESSFIT FEM ST FX 16 X 1 Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6 DEGREE COCR FEM HEAD (various sizes) and 6 DEG UNIPOLAR FEMORAL HE...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.7 X 6 CORT SCREW/SELFTA 2.7 X 7 CORT SCREW/SELFTA Recalled by Zimmer, Inc....
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSYS HERITAGE FEM STEM Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Visible particles embedded in the glass...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.5% Bupivacaine HCl and Epinephrine 1:200 Recalled by Hospira Inc. Due to...
The Issue: Lack of assurance of sterility; equipment failure led to potential breach in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fosinopril Sodium and Hydrochlorothiazide Tablets Recalled by Sandoz Inc Due...
The Issue: Subpotent; Hydrochlorothiazide at the 9 month time point.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daunorubicin Hydrochloride Injection Recalled by Teva Pharmaceuticals USA...
The Issue: Presence of Precipitate; precipitation of drug product
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.