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. 2,510 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,510 in last 12 months

Showing 1292112940 of 27,462 recalls

Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 91mm Item # 195761 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2019· WOM World of Medicine AG

Recalled Item: Aquilex Fluid Control System component: Bag deflector Recalled by WOM World...

The Issue: The deficit displayed by the pump can differ from the real deficit, leading...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2019· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM anti-CCP IgG (aCCP) Assay Siemens Material Number: 10732998...

The Issue: Atellica IM anti-CCP IgG (aCCP) Test Definition (TDef) Mitigation...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: AssayTip/AssayCup Tray-used on the cobas e 801 module which is Recalled by...

The Issue: AssayTips part of the AssayTip/AssayCup Tray Tips used on the cobas e 801...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2019· Baxter Healthcare Corporation

Recalled Item: EXACTAMED Oral Dispensers Recalled by Baxter Healthcare Corporation Due to...

The Issue: Exactamed 5 mL Oral Dispenser Pharmacy Packs may contain both 5 mL and 3 mL...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceAugust 12, 2019· Zeus Scientific, Inc.

Recalled Item: ZEUS ELISA Parvovirus B19 IgM Test System Recalled by Zeus Scientific, Inc....

The Issue: FDA inspection identified that due to increased positivity (false positives)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2019· Varian Medical Systems, Inc.

Recalled Item: Varian Multileaf Collimator [MLC] Recalled by Varian Medical Systems, Inc....

The Issue: After a recent upgrade to the collimator software version 8.5, the firm...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Medtronic Navigation, Inc.

Recalled Item: Medtronic Nexframe Stereotactic System and StealthStation Cranial software...

The Issue: Entry point and lead placement inaccuracies during deep brain stimulation...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Esthetic Abutment CC RP 1.5 mm pre-manufactured prosthetic components...

The Issue: Packages of abutments may contain an incorrect screw. While the screw will...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Temporary Abutment Engaging CC RP pre-manufactured prosthetic components...

The Issue: Packages of abutments may contain an incorrect screw. While the screw will...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Universal Base CC RP 1.5 mm Recalled by Nobel Biocare Usa Llc Due to...

The Issue: Packages of abutments (universal base) may contain an incorrect screw. While...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Temporary Snap Abutment Engaging CC RP 1.5 mm Recalled by Nobel Biocare Usa...

The Issue: Packages of abutments may contain an incorrect screw. While the screw will...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Temporary Abutment Non-Engaging CC RP pre-manufactured prosthetic components...

The Issue: Packages of abutments may contain an incorrect screw. While the screw will...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Snappy Abutment 5.5 CC RP 3 mm Recalled by Nobel Biocare Usa Llc Due to...

The Issue: Packages of abutments may contain an incorrect screw. While the screw will...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Randox Laboratories Ltd.

Recalled Item: Liquid Protein Calibrators (SP CAL (LIQ)) Catalogue Number: IT2691 GTIN:...

The Issue: The assigned value for Rheumatoid Factor over recovers against the material...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Randox Laboratories Ltd.

Recalled Item: Rheumatoid Factor Standard (RF CAL) Catalogue Number: RF2301 GTIN:...

The Issue: The assigned value for Rheumatoid Factor over recovers against the material...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· GE Healthcare, LLC

Recalled Item: Proteus XR/a (SlOK : K993090) Recalled by GE Healthcare, LLC Due to...

The Issue: Intermittently not receiving an audible exposure indication upon completion...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Medline Industries Inc

Recalled Item: Medline SYRINGE Recalled by Medline Industries Inc Due to Samples in the...

The Issue: Samples in the identified lot were found to have incomplete or open...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2019· Radiometer Medical ApS

Recalled Item: AQURE basic sytem Recalled by Radiometer Medical ApS Due to The firm has...

The Issue: The firm has become aware that there is a potential problem relating to the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2019· Intersurgical Inc

Recalled Item: Superset with 22MM ID Recalled by Intersurgical Inc Due to The port may...

The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing