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 2562125640 of 27,462 recalls

Medical DeviceMarch 14, 2013· Synvasive Technology Inc

Recalled Item: The Oxford Partial Knee Recalled by Synvasive Technology Inc Due to Biomet...

The Issue: Biomet part # 506076, lot 928182 was received from Synvasive Technology...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2013· Elekta, Inc.

Recalled Item: Precise Treatment Table. To be used as part of radiation Recalled by Elekta,...

The Issue: The Column rotation can accidentally be moved to a different position which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products PHBR (Phenobarbital) Slides Recalled by...

The Issue: Ortho Clinical Diagnostics (OCD) received customer complaints of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Duraflo coated Femoral Cannula. Product Usage: The...

The Issue: Two unsealed pouches were found at an Edwards' distribution location in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Vitamin D Calibrator 6-pack Recalled by Siemens Healthcare...

The Issue: Negative bias in patient samples for Vitamin D

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Masimo Corporation

Recalled Item: Rad-8 Pulse Oximeters The Rad-8 family of pulse oximeters and Recalled by...

The Issue: Masimo has identified a very small number (0.02%) of Rad-8 devices with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Vitamin D Assay (100 tests) Recalled by Siemens Healthcare...

The Issue: Negative bias in patient samples for Vitamin D

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Separation Technology, Inc.

Recalled Item: SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE. Produce a monolayer of cells...

The Issue: Separation Technology, Inc. recalled SlidePrep Plus Cytology Centrifuges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Epocal

Recalled Item: epoc BGEM Test Card (Catalogue number CT-1004-00-00). quantitative testing...

The Issue: This recall is being initiated because the affected lots of this product may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Vitamin D Assay (500 tests) Recalled by Siemens Healthcare...

The Issue: Negative bias in patient samples for Vitamin D

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Vitamin D Calibrator 2-pack Recalled by Siemens Healthcare...

The Issue: Negative bias in patient samples for Vitamin D

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Archer 0.035 inch (0.89mm) Super Stiff Guidewire Recalled by...

The Issue: Medtronic has identified an issue involving specific lot numbers of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2013· Berchtold Corp.

Recalled Item: Hand Controls for Operon D750 Recalled by Berchtold Corp. Due to The firm...

The Issue: The firm received complaints for unintended movements.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT 16-Slice Water Recalled by Philips Medical Systems (Cleveland)...

The Issue: Philips Healthcare received a report from the field stating when they viewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2013· Custom Ultrasonics, Inc.

Recalled Item: Custom Ultrasonics System 83 Plus 2 and Plus 9 Endoscope Washer/Disinfector....

The Issue: Certain System 83 Plus 2 and System 83 Plus 9 units running the Windows 7...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2013· GE Healthcare It

Recalled Item: The Centricity Laboratory System is intended to be an information Recalled...

The Issue: GE Healthcare has become aware of a potential safety issue associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2013· Lifescan Inc

Recalled Item: All OneTouch Verio IQ Blood Glucose Meters sold as: Verio Recalled by...

The Issue: The Verio IQ meter will shut off and revert to set up mode at glucose values...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 11, 2013· Becton Dickinson & Co.

Recalled Item: BBL(tm) CDC Anaerobe 5% Sheep Blood Agar. Used for culturing microorganisms....

The Issue: Microbiological media may be contaminated with bacteria.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2013· GE Healthcare It

Recalled Item: Centricity Perinatal and Centricity Intensive Care is intended to be...

The Issue: 1) Under rare network conditions, a Centricity Perinatal process may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2013· Becton Dickinson & Co.

Recalled Item: BBL(tm) Trypticase (tm) Soy Agar with 5% Sheep Blood. Used Recalled by...

The Issue: Microbiological media may be contaminated with bacteria.

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

Class II — Potential Health HazardOngoing