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 25661–25680 of 27,462 recalls
Recalled Item: Alaris PC unit model 8015 with software version 9.12 Product Recalled by...
The Issue: The recall was initiated because Carefusion has identified potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIGEN (TM) L-P SCREW Recalled by Smith & Nephew Inc Due to One batch of 4.5...
The Issue: One batch of 4.5 mm diameter Trigen Low-Profile Bone Screws were incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a...
The Issue: Unapproved medical device
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare Diagnostics Inc. MIcroScan MICroSTREP plus Type 1...
The Issue: Customer complaint investigation confirmed the issue of false skipped wells...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Cholestech LDX ALT AST Test Cassette Recalled by Alere San Diego, Inc....
The Issue: The recall was initiated because Alere San Diego has an update for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit model 8015 with software version 9.12 Product Recalled by...
The Issue: The recall was initiated because Carefusion has received reports of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntellVue Info Center iX 866023 Recalled by Philips Healthcare Inc....
The Issue: If a customer creates customized trend scales in the trend review tile and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1488 HD 3-Chip Inline Camera Recalled by Stryker Endoscopy Due to In certain...
The Issue: In certain operating room environments, a colored screen image occurs with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1488 HD 3-Chip Camera Recalled by Stryker Endoscopy Due to In certain...
The Issue: In certain operating room environments, a colored screen image occurs with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1488 HD 3-Chip Camera Recalled by Stryker Endoscopy Due to In certain...
The Issue: In certain operating room environments, a colored screen image occurs with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20-Pole Eco Cable Recalled by Biosense Webster, Inc. Due to Biosense is...
The Issue: Biosense is recalling the 20-Pole Eco Cable because it was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuViz Dual series CT Scanner System Recalled by Philips And Neusoft Medical...
The Issue: User error of the NeuViz 16 or NeuViz Dual may cause personnel injuries....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quick Connect QLC1677E Recalled by Steris Corporation Due to During a...
The Issue: During a routine label review, the firm identified four SYSTEM 1E Quick...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens syngo.plaza SW version VA20 with Mammography license. image...
The Issue: Siemens issued a Customer Safety Notice to inform customers of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sepp Recalled by CareFusion 213, LLC Due to An internal review of...
The Issue: An internal review of CareFusion's labeling for preoperative skin prep...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuViz 16 Multi-Slice CT Scanner System Recalled by Philips And Neusoft...
The Issue: User error of the NeuViz 16 or NeuViz Dual may cause personnel injuries....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche Molecular Systems cobas x 480 System 50 mL reagent reservoir Recalled...
The Issue: Certain lots of Reagent reservoirs, may not have a separation in the lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diacap(R) Ultra Dialysis Fluid Filter Recalled by B. Braun Medical, Inc. Due...
The Issue: There is the potential of the residual moisture of the Diacap Ultra membrane...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...
The Issue: American Medical Systems, Inc. is initiating a recall on two components of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...
The Issue: American Medical Systems, Inc. is initiating a recall on two components of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.