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. 2,529 recalls have been distributed to Wyoming in the last 12 months.
Showing 11301–11320 of 27,462 recalls
Recalled Item: Alaris Syringe Module Model 8110 Recalled by CareFusion 303, Inc. Due to...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pleur-Evac Adult-Ped Wet Recalled by TELEFLEX MEDICAL INC Due to Potential...
The Issue: Potential for sterile packaging to be compromised¿
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressa Bed Recalled by Hill-Rom, Inc. Due to Affected beds may have...
The Issue: Affected beds may have screws installed that do not meet material tensile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearPro Trach T-Piece Closed Suction Catheter Recalled by Medline...
The Issue: There are reports of the suction catheter coming apart from the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centrella Smart+ Bed Recalled by Hill-Rom, Inc. Due to Affected beds may...
The Issue: Affected beds may have screws installed that do not meet material tensile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearPro T-Piece Closed Suction Catheter Recalled by Medline Industries Inc...
The Issue: There are reports of the suction catheter coming apart from the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERI-LOC TARGETER 4.5MM DISTAL FEMUR Recalled by Smith & Nephew, Inc. Due to...
The Issue: The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PVA Recalled by Precision Valve & Automation,Inc Due to While operating the...
The Issue: While operating the machine in "Run" mode an unexcepted event may occur...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOSS DeBakey "Gator-Grip" Needle Holder 2 mm tip Recalled by Boss...
The Issue: The tungsten carbide plate, which is intended to hold the sewing needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Lipase Assay: Lipase Colorimetric R2 Substrate - Product Usage:...
The Issue: Randox have confirmed imprecision of quality control and patient samples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Lipase Assay: Lipase Colorimetric R1 Buffer - Product Usage: Recalled...
The Issue: Randox have confirmed imprecision of quality control and patient samples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Lipase Assay: Lipase Colorimetric Reagent - Product Usage: A Recalled...
The Issue: Randox have confirmed imprecision of quality control and patient samples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InnoWave Sonic Irrigator Recalled by Steris Corporation Due to A recent FDA...
The Issue: A recent FDA inspection at the firm identified that the foil test performed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue G7m Anesthesia Gas Module Recalled by Philips North America, LLC...
The Issue: The device may experience an interruption of gas measurement due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepIT Q2A Kit Recalled by DNA Genotek Inc. Due to Reagents were shipped to...
The Issue: Reagents were shipped to customers after the Use by data indicated on its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew T-F1X0 RCG Drill Pac Recalled by Smith & Nephew, Inc. Due to...
The Issue: The T-Fix sterile package contains only one sleeve instead of two, The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite with software versions syngo.via VB30 or VB40...
The Issue: If the user modifies for any reason (e.g. reduction of artifacts) the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TTDEYE (brand) Radial Pink Recalled by Chengdu Ai Qin E-commerce Co., Ltd...
The Issue: Colored contact lenses were distributed without FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutter Swyng non-stick bipolar forceps - Product Usage: single-use re...
The Issue: The label on the cardbox and the blister show the correct symbols for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TTDEYE (brand) Radial Brown Recalled by Chengdu Ai Qin E-commerce Co., Ltd...
The Issue: Colored contact lenses were distributed without FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.