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.

48,219 total recalls
2,378 in last 12 months

Showing 2600126020 of 27,462 recalls

Medical DeviceDecember 12, 2012· Abbott Laboratories

Recalled Item: Abbott Laboratories Recalled by Abbott Laboratories Due to The Architect...

The Issue: The Architect 25-OH Vitamin D assay has the potential to generate falsely...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2012· Toshiba American Medical Systems Inc

Recalled Item: Aplio 500/400/300 Diagnostic Ultrasound System (TUS-500/400/300). Device...

The Issue: Toshiba Medical Systems has received reports of startup issues with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2012· Becton Dickinson & Co.

Recalled Item: BBL(TM) Fildes Enrichment Recalled by Becton Dickinson & Co. Due to...

The Issue: Enrichment media intended to enhance the cultivation of various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2012· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: Flowtron Trio DVT Pump Recalled by Arjo, Inc. dba ArjoHuntleigh Due to The...

The Issue: The Flowtron Trio DVT Pump has been marketed without proper FDA Approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2012· Hill-Rom, Inc.

Recalled Item: Liko Standard Slingbar 450. The Standard Slingbar 450 is a Recalled by...

The Issue: Liko/Hill-Rom has received reports from facilities which indicate that...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Emit(R) tox(TM) Serum Calibrators Recalled by Siemens Healthcare...

The Issue: Incorrect expiration date was assigned to the D1 lot of Emit(R) tox(TM)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 5, 2012· SynCardia Systems Inc.

Recalled Item: Companion External Battery Recalled by SynCardia Systems Inc. Due to...

The Issue: Syncardia Systems is recalling the Companion External Batteries used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2012· Canon Inc.

Recalled Item: Canon Full Auto RK-F2 Recalled by Canon Inc. Due to Canon Inc. had received...

The Issue: Canon Inc. had received 17 claims from our foreign sales companies between...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2012· B Braun Medical, Inc.

Recalled Item: Outlook ES pump is intended for use with B. Braun Recalled by B Braun...

The Issue: B. Braun Medical Inc. is informing our customers of a field correction...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2012· Abbott Molecular

Recalled Item: Abbott m2000sp Instrument Recalled by Abbott Molecular Due to An issue with...

The Issue: An issue with the m2000sp Instrument software has been identified whereby,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS 8IN CALC 1.5/18.0 Packaging: Product is packed within Recalled by...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS L 9IN CALC 2.25/15.0 Packaging: Product is packed Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· Quidel Corporation

Recalled Item: Quidel Recalled by Quidel Corporation Due to Quidel Corporation has...

The Issue: Quidel Corporation has initiated a voluntary recall of specific lots of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS R 9IN CALC 2.25/16.5 Packaging: Product is packed Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS 8IN CALC 1.5/19.5 Packaging: Product is packed within Recalled by...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS L 9IN CALC 2.25/19.5 Packaging: Product is packed Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· Medtronic Neuromodulation

Recalled Item: Medtronic Recalled by Medtronic Neuromodulation Due to Medtronic has...

The Issue: Medtronic has identified 140 Restore DBS Extension Kits (model numbers 7482,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS F 8 CALC 13.5MM LG Packaging: Product is Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS R 9IN CALC 2.25/18 Packaging: Product is packed Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS R 9IN CALC 2.25/21 Packaging: Product is packed Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing