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. 2,415 recalls have been distributed to Wyoming in the last 12 months.
Showing 19981–20000 of 27,462 recalls
Recalled Item: LightSpeed 16 (MDAS only Recalled by GE Medical Systems, LLC Due to GE...
The Issue: GE Healthcare has updated the Service Manuals for a number of CT and PET CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery ST Recalled by GE Medical Systems, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has updated the Service Manuals for a number of CT and PET CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra 8 IAB: 8Fr 30cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightSpeed QX/I (4-slice MDAS) LightSpeed 4.0 CT Scanner System - Recalled...
The Issue: GE Healthcare has updated the Service Manuals for a number of CT and PET CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RediGuard IAB: 7Fr 30cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraFlex IAB: 7.5Fr 30cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FiberOptix Ultra 8 IAB: 8Fr 30cc The Arrow¿ IAB is Recalled by Arrow...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightSpeed Plus (4-slice MDAS LightSpeed 4.0 CT Scanner System - Recalled by...
The Issue: GE Healthcare has updated the Service Manuals for a number of CT and PET CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraFlex IAB: 7.5Fr 40cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Insertion Tray Recalled by Arrow International, Inc., Division...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FiberOptix Ultra 8 IAB: 8Fr 40cc Recalled by Arrow International, Inc.,...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. The firm name on the label is Merge Healthcare...
The Issue: A report can be confirmed with the incorrect patient demographics resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J...
The Issue: Bard Peripheral Vascular, Inc. is recalling Denali Filter-Jugular/Subclavian...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Denali Filter-Femoral Delivery System Product Code: DL900F/DL950F Recalled...
The Issue: Bard Peripheral Vascular, Inc. is recalling Denali Filter-Jugular/Subclavian...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TF Adaptive Gutta Percha Point Size SM3 50pk Recalled by Ormco/Sybronendo...
The Issue: Ormco Corporation is recalling the TF Adaptive Gutta Percha Point Size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroAire PAL-R4011XL - 40cm x 4 mm Del Vecchio French Rasp aspiration...
The Issue: Complaints that the cannula bent/broke during surgery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroAire PAL¿ Cannula Product Usage - Power Aspiration Device Recalled by...
The Issue: MicroAire has initiated a recall on product PAL-R4011XL (40cm x 4mm Del...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano R100 Sterile Equipment Cover Recalled by Volcano Corporation Due to...
The Issue: Volcano Corporation has identified that certain lot numbers of Volcano R-100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano SpinVision Sterile Equip cover II Recalled by Volcano Corporation...
The Issue: Volcano Corporation has identified that certain lot numbers of Volcano R-100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allegra X-5 rotor yoke Recalled by Beckman Coulter Inc. Due to A defective...
The Issue: A defective rotor yoke on Allegra X-5 allows improper rotor seating on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.