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. 2,383 recalls have been distributed to Wyoming in the last 12 months.
Showing 24201–24220 of 27,462 recalls
Recalled Item: S3 Med/Surg Bed Secure II and the 3002 S3 are Recalled by Stryker Medical...
The Issue: Stryker Medical has identified a potential issue associated with Secure II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Secure II Med/Surg Bed Secure II and the 3002 S3 Recalled by Stryker Medical...
The Issue: Stryker Medical has identified a potential issue associated with Secure II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agility. Version 3.1 of the Integrity interface and control software...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XiO RTP System. Used to create treatment plans for any Recalled by Elekta,...
The Issue: When bolus is present, the Effective Depth (with bolus) to the weight point...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HT Connect Peripheral Guide Wire Part Number Description 1012587 018...
The Issue: Abbott Vascular has initiated a recall of the HT Connect Peripheral Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DR 7500 with FF WS These products are permanently installed Recalled by...
The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Evolution with CSH WS These products are permanently installed...
The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Port Kit with Access Infusion Set under the following labels: Recalled by...
The Issue: Navilyst Medical has recalled a Port Kit with Access Infusion Set due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viscocel and Viscocel Plus. These products are intraocular fluid devices...
The Issue: CLR Medicals International Inc., initiated a nationwide recall of Viscocel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Evolution with FF WS These products are permanently installed diagnostic...
The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrity. Version 1.1 of the Integrity interface and control software...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Desktop Pro TM linear accelerator control software intended to assist...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agility. Version 3.0 of the Integrity interface and control software...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy XVI The Elekta Synergy S is intended to be Recalled by Elekta, Inc....
The Issue: Potential collision risk when using XVI and external beam shaping devices.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy XVI XVI can incorrectly calculate the target position of Recalled by...
The Issue: XVI can incorrectly calculate the target position of the treatment table.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-10 Dual Program Recalled by Bio-Rad Laboratories, Inc. Due to D-10 A1c...
The Issue: D-10 A1c Dual Program Floppy was programmed incorrectly and cartridge...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion¿ 4000 Syringe Infusion Pumps Medfusion¿ 4000 Syringe Infusion...
The Issue: Smiths Medical is conducting a recall involving all Medfusion¿ 4000 Syringe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Testing Disc Recalled by Remel Inc Due to...
The Issue: Individual discs in the lot may not be sufficiently impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision R C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision(2) FD C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.