Product Recalls in West Virginia
Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,029 recalls have been distributed to West Virginia in the last 12 months.
Showing 16041–16060 of 48,376 recalls
Recalled Item: Sulfur Ointment 10% Recalled by DLC Laboratories, Inc Due to Labeling: Label...
The Issue: Labeling: Label Mix-Up. THe English label with Drug Facts panel for Camphor...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Infusion Pump Recalled by Baxter Healthcare Corporation Due to Battery...
The Issue: Battery performance issues related to prolonged storage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHILIPS BATTERY Recalled by Respironics California, LLC Due to Due to...
The Issue: Due to unqualified "design verification" batteries being shipped to customers.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit 7Fr 3 Lumen- Intended for Recalled by Arrow...
The Issue: The lidstock / information card on the kits correctly states the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9180 Electrolyte Analyzer - Product Usage: intended to be used Recalled by...
The Issue: May display Calcium results on the screen with wrong arrow direction which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cascade Abrazo aPTT Test Card - Product Usage: are to Recalled by Helena...
The Issue: Intermittent potential for shorter than expected clot times.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Klein s Vanilla Ice Cream. Packaged in a 3 gallon paper drum. Recalled by...
The Issue: Ice Cream product may contain metal (foreign objects).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Klein s Cookies and Cream Bulk Packaged in a 3 gallon paper drum. Recalled...
The Issue: Ice Cream product may contain metal (foreign objects).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Weis Quality Cookies and Cream Ice Cream (48oz). Packaged in Recalled by...
The Issue: Ice Cream product may contain metal (foreign objects).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nelsons Graham Slam Bulk. Packaged in a 3 gallon paper drum. Recalled by...
The Issue: Ice Cream product may contain metal (foreign objects).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PBD-203-0707 BILIARY STENT Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NA-401D-1521 ASPIRATION NEEDLE Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEEDLEMASTER 6MMx 25G LOWER Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KD-655L ELECTROSURGICAL SNARE Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B7-2C BALLOON CATHETER 13mm dia 2.8 Recalled by Aomori Olympus Co., Ltd. Due...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX LOWER 25G 5MM Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEEDLEMASTER 4MMx 26G LOWER Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX LOWER 23G 5MM Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SD-400U-10 SNAREMASTER PLUS Hot/Cold 10m Recalled by Aomori Olympus Co.,...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEEDLEMASTER 6MMx 21G UPPER Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.