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. 2,503 recalls have been distributed to Wyoming in the last 12 months.
Showing 14761–14780 of 27,462 recalls
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott ARCHITECT cSystems ICT Module Recalled by Abbott Laboratories, Inc...
The Issue: There is a potential to generate falsely elevated serum or plasma chloride...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyPass System 241-S Recalled by Alcon Research, LTD. Due to Analysis of the...
The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo 100/120V AC Recalled by Terumo Cardiovascular Systems Corporation Due...
The Issue: Screws on a Terumo¿ Advanced Perfusion System 1 Power Manager Board (the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyPass System 241 Recalled by Alcon Research, LTD. Due to Analysis of the...
The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Li-ion Battery Housing for AR-400 DrillSaw Sports 400 System Product...
The Issue: The Li-ion Battery Housing for the AR-400 DrillSaw Sports 400 System may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco DPBS Recalled by Life Technologies, Corp. Due to Leaky bottles due to...
The Issue: Leaky bottles due to a defect in the bottle cap compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco GlutaMAX Supplement Recalled by Life Technologies, Corp. Due to Leaky...
The Issue: Leaky bottles due to a defect in the bottle cap compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco Sodium Pyruvate (100 mM) SKU 11360070 Recalled by Life Technologies,...
The Issue: Leaky bottles due to a defect in the bottle cap compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco MEM Non-Essential Amino Acids Solution (100X) (SKU 11140050) Recalled...
The Issue: Leaky bottles due to a defect in the bottle cap compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrated Gate Controller PCB (component of AlignRT Plus) Truebeam variant...
The Issue: RTInterface error in the event of an I/O error between the IGC PCB and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Uric Acid Recalled by Beckman Coulter Inc. Due to NAPQI, a...
The Issue: NAPQI, a metabolite of Acetominophen, causes negative interference with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Lipase Recalled by Beckman Coulter Inc. Due to NAPQI, a...
The Issue: NAPQI, a metabolite of Acetaminophen, causes negative interference with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-360 Analyzer Recalled by Tosoh Bioscience Inc Due to The firm has...
The Issue: The firm has implemented new product labeling changes for the Tosoh AIA-360...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD NEXIVA Closed IV Catheter System Dual Port 18GA 1.25 IN (BD Nexiva...
The Issue: One lot of the specified needles is not performing as intended due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp :...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.