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. 2,466 recalls have been distributed to Wyoming in the last 12 months.
Showing 17461–17480 of 27,462 recalls
Recalled Item: CD117 Recalled by Cell Marque Corporation Due to Cell Marque has determined...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adenovirus (20/11 & 2/6) Recalled by Cell Marque Corporation Due to Cell...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Herpes Simplex Virus II 0.5 ml catalog number 362A-15 7.0 Recalled by Cell...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Her2/Neu (EP3) Recalled by Cell Marque Corporation Due to Cell Marque has...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Herpes Simplex Virus I Recalled by Cell Marque Corporation Due to Cell...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varicella Zoster Virus 7.0 ml catalog number 364M-18 Microbiology - Recalled...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H. pylori (polyclonal} 1.0 mL Catalog number 215A-76 Recalled by Cell Marque...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HHV-8 (13810) Recalled by Cell Marque Corporation Due to Cell Marque has...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arsenal Spinal Fixation System Recalled by Alphatec Spine, Inc. Due to...
The Issue: Alphatec Spine is recalling the Arsenal Spinal Fixation System Set Screw due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Her2/Neu (c-erbB-2) (CB-1 1) Recalled by Cell Marque Corporation Due to Cell...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estrogen Receptor (EP1) 7.0 mL Catalog number 249R-28 Recalled by Cell...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Opteryx Variable Rescue Screw Recalled by Innovasis, Inc Due to Opteryx...
The Issue: Opteryx Variable Rescue Screws are engraved with incorrect (larger) size (16...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SV40 (MRQ-4) 0.5 ml catalog number 351 M-15. Microbiology - Recalled by Cell...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant Warmer System (IWS) Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures. MAXON: MAXON 4/0 5X18" GREEN CV-24 D-TACH Recalled by Medtronic Due...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures. POLYSORB: POLSORB 0 18 U/D PRECUT 126R Recalled by Medtronic Due to...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures. BIOSYN: BIOSYN 4/0 18" VIOLET CV-25 DT Recalled by Medtronic Due to...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures. ENDO STITCH: ENDO STITCH POLYSORB 0 48" U/D DLU SU Recalled by...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCHRITTMACHER ANGIO X3 Recalled by Medtronic Due to Potential for an...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OptiLite Multi-Use Holmium Laser Fibers Recalled by Cook Inc. Due to Cook...
The Issue: Cook Inc. is initiating a voluntary recall of the OptiLite Multi-Use Holmium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.