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. 2,450 recalls have been distributed to West Virginia in the last 12 months.
Showing 18641–18660 of 27,884 recalls
Recalled Item: XCELA PASV 5F DL 55CM MST-70 KIT PG Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved w/ Nit GW Recalled by...
The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved PG Recalled by Angiodynamics...
The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved PG Recalled by Angiodynamics...
The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NucliSENS magnetic extraction reagents Recalled by BioMerieux SA Due to A...
The Issue: A drift of the performance with the BK test (BK virus, worst case...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unna-Z Recalled by Medline Industries Inc Due to Medline Industries, Inc is...
The Issue: Medline Industries, Inc is recalling Unna Z Unna Boot Bandage 3 X10 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MagSIL (NucliSENS easyMAG Magnetic Silica) Recalled by BioMerieux SA Due to...
The Issue: A drift of the performance with the BK test (BK virus, worst case...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Drill 1 Recalled by Straumann Manufacturing, Inc. Due to Drills...
The Issue: Drills cannot be inserted into handpiece due to tolerance specification not met
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Twist Drill PRO ¿4.2mm Recalled by Straumann Manufacturing, Inc....
The Issue: Drills cannot be inserted into handpiece due to tolerance specification not met
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Savannah-T Straight Rod Recalled by Amendia, Inc Due to The rods are...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Recalled by Teleflex Medical Due to Labeling Inconsistency: The...
The Issue: Labeling Inconsistency: The products have been labeled with the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire 1.4mm x 12in Non-Threaded Recalled by Amendia, Inc Due to The rods...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durex Pleasure Pack . 3 ultra fine lubricated latex condoms Recalled by...
The Issue: Reckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Widow 6.6mm x 20mm Screw Recalled by Amendia, Inc Due to There is a...
The Issue: There is a problem with the mating feature between the plate and screw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G3 Opticage Expandable Interbody Fusion Device Recalled by Interventional...
The Issue: During implantation, the proximal end of the device could separate if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Widow Plate 19mm Plate Recalled by Amendia, Inc Due to There is a...
The Issue: There is a problem with the mating feature between the plate and screw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS IMMULITE 2000/2000 Xpi Systems Intact PTH (Parathyroid Hormone) Test...
The Issue: Siemens is conducting this recall for the IMMULITE¿ 2000/IMMULITE¿ 2000 XPi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Stylet Needle Recalled by Amendia, Inc Due to The rods are packaged in...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Legacy Recalled by GE Healthcare, LLC Due to GE Healthcare is conducting a...
The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceramax Skin Barrier Cream: NET WT 0.1 OZ (3 g Recalled by Oculus Innovative...
The Issue: Firm became aware that professional samples of Ceramax are not meeting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.