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. 2,356 recalls have been distributed to West Virginia in the last 12 months.
Showing 25281–25300 of 48,376 recalls
Recalled Item: Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia Recalled by...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA 45mm Curved Tip Articulating Vascular/Medium Reload with Tri-Staple...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Staple 2.0 Intelligent Reload for use with Signia stapling system...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA 45 mm Articulating Medium/Thick Reload with Tri-Staple Technology...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: READYFLUSH PROTECT with Dimethicone (3.2%) Recalled by Medline Industries...
The Issue: Microbial Contamination of a Non-Sterile Product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol Recalled by Lake...
The Issue: Lake Michigan Distilling, LLC, dba Ethanol Extraction has initiated a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Broccoli cuts Recalled by Ahold USA Due to Potential Listeria Contamination
The Issue: Ahold Delhaize received a report from State of CT of finding significant...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ingenuity Digital PET/CT System Recalled by Philips Medical Systems...
The Issue: The block used to connect the patient pallet to the couch may be assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNI Hip System Recalled by OMNIlife science Inc. Due to The Internal...
The Issue: The Internal packaging, the pouch and patient labels are improperly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmniSure ROM Test under the following labels: 1) Catalog Number Recalled by...
The Issue: Potential for control line not appearing on the test strip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Recalled...
The Issue: Natus Neuro has discovered a possible manufacturing defect in the ErgoJust...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPS Rhythm ECG Accessory Pack with Johans Adapter Recalled by Arrow...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peripherally Inserted Midline Catheter Kit with Placement Wire Recalled by...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPS Rhythm ECG Accessory Pack Recalled by Arrow International Inc Due to...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPS TipTracker Stylet Accessory Recalled by Arrow International Inc Due to...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POSEIDON Xtreme PLATINUM 4500 Recalled by Shoreside Enterprises Inc. Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found products to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 7K capsules packaged in single packs sold in 24-count boxes Recalled by...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found products to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: My Way (levonorgestrel) Tablets TWO PACK Recalled by Lupin Pharmaceuticals...
The Issue: Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: My Way (Levonorgestrel) Tablets TWO PACK Recalled by Lupin Pharmaceuticals...
The Issue: Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: screamin' menthol (menthol) Pain Relieving Gel Recalled by Ideaz Llc Due to...
The Issue: CGMP Deviations: Products manufactured with an ingredient that exceed the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.