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. 2,378 recalls have been distributed to Wyoming in the last 12 months.
Showing 25841–25860 of 27,462 recalls
Recalled Item: Prism Medical C-Series Carry Bar Recalled by Prism Medical Services USA Due...
The Issue: The firm replaced the recalled carry bar with a plastic insert with a carry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KY SENSITIVE TM JELLY Personal Lubricant. The product is packaged Recalled...
The Issue: This product is not cleared for marketing in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 840 Series Ventilator PB840 Operators Manual Addendum PN...
The Issue: Covidien is correcting labeling to clarify the operational life of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proplege Coronary Sinus Catheter model PR9 Recalled by Edwards Lifesciences,...
The Issue: Edwards Lifesciences is recalling certain Proplege Coronary Sinus Catheter,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KY SilkE Vaginal Moisturizer and Personal Lubricant. The product is Recalled...
The Issue: This product is not cleared for marketing in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 700 Series Ventilators (PB740 and PB760) PB700 Series...
The Issue: Covidien is correcting labeling to clarify the operational life of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KY TINGLING JELLY Personal Lubricant. The product is packaged into Recalled...
The Issue: This product is not cleared for marketing in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D3000I Advantage Drive System Recalled by Linvatec Corp. dba ConMed Linvatec...
The Issue: The Membrane Switch Panel ( to as "front panel" of the component part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D3000 Advantage Drive System Recalled by Linvatec Corp. dba ConMed Linvatec...
The Issue: The Membrane Switch Panel ( to as "front panel" of the component part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLD System Recalled by Cenorin, LLC Due to The temperature sensor/control...
The Issue: The temperature sensor/control system in the HLD Systems Model 610 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stelkast Cross-over Acetabular Shell and Liner Hip System Recalled by...
The Issue: Firm was made aware of incidents relating to the difficulty of properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD Biopsy Systems (A Business Unit of Bard Peripheral Vascular Recalled by...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: USHER¿ Support Catheter- Angled Tip WL130cm Recalled by Bard Peripheral...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic bottle containing 3.5 mL of IgG FITC Conjugate Product Recalled by...
The Issue: Affected products have a labeled expiration date of one year too long.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic bottle containing 10.5 mL of IgM Conjugate Product Usage: Recalled...
The Issue: Affected products have a labeled expiration date of one year too long.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROSHEATH¿ - 0.066 (1.7mm) proximal Recalled by Bard Peripheral Vascular...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD Biopsy Systems (A Business Unit of Bard Peripheral Vascular Recalled by...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic bottle containing 10.5 mL of IgG Conjugate Product Usage: Recalled...
The Issue: Affected products have a labeled expiration date of one year too long.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lifeguard Infusion Set with Smartsite Recalled by Churchill Medical Systems,...
The Issue: The label on the device states that the item number is CLGY-2210 when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Advantx Recalled by GE Healthcare, LLC Due to A locking nut...
The Issue: A locking nut might loosen out of the overhead Video Monitor Suspension yoke...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.