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. 2,448 recalls have been distributed to Wyoming in the last 12 months.
Showing 17941–17960 of 48,219 recalls
Recalled Item: PENTARAY NAV HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx only Recalled...
The Issue: Mapping Catheter can become entrapped in the cardiac valvular apparatus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTARAY NAV eco HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx Recalled...
The Issue: Mapping Catheter can become entrapped in the cardiac valvular apparatus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Pheno - Interventional Fluoroscopic X-Ray System Model: 10849000 -...
The Issue: If the C-arm leaves its intended travel path due to a fault within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infuvite PEDiatric Pharmacy Recalled by Sandoz, Inc Due to Defective...
The Issue: Defective Container: Sub-optimal crimping in vial of Pediatric Infuvite...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BioPlex 2200 Syphilis Total & RPR Linked Immunoabsorption Assay Recalled by...
The Issue: The increased level of RPR reactivity in the BioPlex 2200 Syphilis Total &...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 The Proton Therapy System - Proteus 235 (brand Recalled by Ion...
The Issue: Signature from the user is necessary to proceed with specific actions in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL Monitor/Defibrillators Model number: M4735A - Product...
The Issue: HeartStart XL MonitorlDefibrillators may not have been included in prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketorolac Tromethamine Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Presence of Particulate Matter - found in reserve sample vials at the firm.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Presence of Particulate Matter - found in reserve sample vials at the firm.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Very Berry Recalled by...
The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Pretty in Recalled by...
The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Peachy Keen Recalled by...
The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Product...
The Issue: Product Mix-Up: a complaint received indicating mix-up of 10 mg Lisinopril...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oscar 2 Recalled by Suntech Medical, Inc. Due to The device display, when...
The Issue: The device display, when activated, can show an incorrect decimal point when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard. Item number: 830034. GS0348D- CVC Triple Lumen 20CM non Sulfa-Mercy....
The Issue: Custom procedure kits contains affected lots of PosiFlush Syringe, a product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUE METRIX SELF MONITORING BLOOD GLUCOSE SYSTEM - Product Usage: Recalled...
The Issue: One (1) TRUE METRIX AIR blood glucose meter distributed in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Sterilizable Defibrillator Internal Paddles - Internal paddles are...
The Issue: Internal Paddles may wear over time and may not be safe or ready for use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Renuvion/ J-Plasma Precise Handpiece. Catalog numbers BVX-150B Recalled by...
The Issue: Unexpected stress fractures on the shaft of the hand piece may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Professional Urine Drug Control Recalled by Cardinal Health Inc. Due to...
The Issue: Three products requiring storage conditions were incorrectly stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Renuvion/ J-Plasma Precise Open Handpiece. Catalog numbers BVX-044-BPS...
The Issue: Unexpected stress fractures on the shaft of the hand piece may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.