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. 2,378 recalls have been distributed to Wyoming in the last 12 months.
Showing 25361–25380 of 27,462 recalls
Recalled Item: - ConMed Linvatec Spectrum II Suture Hook Crescent Recalled by Surgical...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harmonic ACE Ergonomically-Enhanced Curved Shear Recalled by Surgical...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Large Tear Cross Cut Rasp 14mm x 7mm Ref. 5100-37-114 Recalled by Surgical...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Glenosphere orientation guide Product Usage: The glenosphere...
The Issue: The Glenosphere Orientation Guide Instrument Used with the Delta XTEND...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PadPro(R) Adult Radiotransparent Multifunction Electrodes Recalled by ConMed...
The Issue: ConMed was notified by the contract manufacturer that their wire/connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - Abrader Bur Recalled by Surgical Instrument Service And Savings, Inc. Due...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical PerfOrma Anglographic Catheter 5F Multipack Product Usage:...
The Issue: Merit Medical Systems is recalling various lots of Performa Cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens brand MicroScan Dried Negative Breakpoint Combo 47 panels...
The Issue: The product has the potential for false negative or delayed reaction for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streptex* kit Recalled by Remel Inc Due to The product may give weak or...
The Issue: The product may give weak or false negative test results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streptex* Latex D Recalled by Remel Inc Due to The product may give weak or...
The Issue: The product may give weak or false negative test results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DMLC IV-ERGO Product Usage: Intended for use with rotating gantry Recalled...
The Issue: It is possible for an intermittent error to occur in the gantry sensor of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD SafetyGlide Allergy. Sterile Allergy Treatment Syringe Tray. Recalled by...
The Issue: There has been an increase in complaints regarding the needle/safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Applied Medicals Epix¿ and Direct Drive Laparoscopic Graspers Recalled by...
The Issue: Applied Medical is conducting a voluntary recall on specific lot numbers of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Multiple Sample and Direct Draw Luer Adapter BD Franklin Lakes...
The Issue: BD Vacutainer Multiple Sample and Direct Draw Luer Adapter may have blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical TransWarmer Infant Transport Mattress with WarmGel P/N 20421...
The Issue: Trans Warmer Infant and Transport Mattress not labeled with exp.date may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics Micro Introducer Kits under the following labeling: 1)...
The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: adult defibrillation Recalled by TZ Medical Inc. Due to TZ Medical Inc is...
The Issue: TZ Medical Inc is recalling its P-211-M1 and P-214-M1 Medtronic / Physio...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SlingBar Wide 670. Designed to meet the needs for lifting humans. Recalled...
The Issue: Retrospective review found 4 sling bars that may present a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FAST Procedure Kit. Intended for use as a Minor Surgical Procedures Tray....
The Issue: American Optisurgical, Inc initiated a recall of ChloraPrep Hi-Lite Orange...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.