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.

48,219 total recalls
2,383 in last 12 months

Showing 2438124400 of 27,462 recalls

Medical DeviceOctober 25, 2013· Hospira Inc.

Recalled Item: *** 1) List number 126970465 labeled in part: 12697-65 LifeShield Recalled...

The Issue: Several lots of the LifeShield Latex-Free HEMA Y-Type Blood Set IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2013· Civco Medical Instruments Inc

Recalled Item: Civco Belly Board MRI Recalled by Civco Medical Instruments Inc Due to...

The Issue: Scales adhered to the product may be misaligned from the zero such that one...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Discovery NMCT 670 Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue related...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Anti-HBs Calibrators & VITROS Anti-HBs Reagent Packs Recalled by...

The Issue: Ortho Clinical Diagnostics issued a Product Correction Notification for...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2013· Biomet, Inc.

Recalled Item: Security (TM) Enclosed Carpal Tunnel System Blade ( Recalled by Biomet, Inc....

The Issue: Security Blades were manufactured oversized and potentially won't advance or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2013· Civco Medical Instruments Inc

Recalled Item: Civco Belly Board Recalled by Civco Medical Instruments Inc Due to Scales...

The Issue: Scales adhered to the product may be misaligned from the zero such that one...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Aviva Combo Blood Glucose Meter (as a part of Recalled by Roche...

The Issue: There is a software synchronization issue with the ACCU-CHEK Combo system....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2013· Varian Medical Systems, Inc.

Recalled Item: C-Series: Clinac Recalled by Varian Medical Systems, Inc. Due to This...

The Issue: This correction is to notify users that a solution to a previous correction...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2013· Nobel Biocare Usa Llc

Recalled Item: Osseocare Pro Console & Set Osseocare Pro Recalled by Nobel Biocare Usa Llc...

The Issue: The recall was initiated because there is a potential for malfunction of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2013· Kimberly-Clark Corporation

Recalled Item: Kimberly-Clark Single Shot Epidural Pain Management Trays containing the BD...

The Issue: Kimberly-Clark Single Shot Epidural Pain Management Trays contain the BD 7...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Stryker Medical Division of Stryker Corporation

Recalled Item: Model FL14E Rose BedsThe Rose Bed is an AC-powered adjustable Recalled by...

The Issue: It was reported that the siderail may appear latched when it is not, due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS brand ONCOR series Linear Accelerator Linac systems with component:...

The Issue: A safety risk regarding a potentially existing dark current radiation...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· ConMed Corporation

Recalled Item: ALTRUS¿ THERMAL TISSUE FUSION Recalled by ConMed Corporation Due to The...

The Issue: The affected lots were exposed to a higher than acceptable level of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Philips Medical Systems, Inc.

Recalled Item: BrightView XCT is a gamma camera for Single Photon Emission Recalled by...

The Issue: It was discovered the CT portion of the scan was interrupted ( stopping the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Carl Zeiss Meditec, Inc.

Recalled Item: Zeiss brand IOLMaster Recalled by Carl Zeiss Meditec, Inc. Due to The user...

The Issue: The user database delivered for download contained an erroneous value....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Carl Zeiss Meditec, Inc.

Recalled Item: Zeiss brand IOLMaster 500 Recalled by Carl Zeiss Meditec, Inc. Due to The...

The Issue: The user database delivered for download contained an erroneous value....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Alere San Diego, Inc.

Recalled Item: Product Brand Name(s): Alere Cholestech LDX¿ Lipid Profile"GLU Test Cassette...

The Issue: Alere initiated a recall of Cholestech LDX Lipid Profile-GLU test cassettes,...

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

Class III — Low RiskOngoing
Medical DeviceOctober 23, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS brand ARTISTE Linear Accelerator Linac systems with component: any...

The Issue: A safety risk regarding a potentially existing dark current radiation...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· ConMed Corporation

Recalled Item: ALTRUS¿ THERMAL TISSUE FUSION Recalled by ConMed Corporation Due to The...

The Issue: The affected lots were exposed to a higher than acceptable level of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: ZINGER¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing