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. 2,330 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,330 in last 12 months

Showing 3988139900 of 48,219 recalls

Medical DeviceJuly 22, 2014· Zimmer, Inc.

Recalled Item: Magna-Fx Cannulated Screw Fixation System Bone Screw Fully Threaded Sterile...

The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Zimmer, Inc.

Recalled Item: 6.5 mm Cancellous Screw Fully Threaded Sterile zimmer Recalled by Zimmer,...

The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Zimmer, Inc.

Recalled Item: Magna-Fx Cannulated Screw Fixation System Cannulated Bone Screw Sterile...

The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Zimmer, Inc.

Recalled Item: 4.0 mm Cancellous Screw Recalled by Zimmer, Inc. Due to Zimmer is recalling...

The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2014· GF Health Products, Inc./d.b.a.Basic American Metal Products

Recalled Item: Zenith Slide W-I-D-E Long Term Care Bed Recalled by GF Health Products,...

The Issue: The bed head deck may fail to elevate as expected during normal operation....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2014· Medtronic MiniMed Inc.

Recalled Item: Medtronic MiniMed Guardian Monitor Recalled by Medtronic MiniMed Inc. Due to...

The Issue: Medtronic MiniMed is recalling the Guardian REAL-Time monitors because of a...

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

Class II — Potential Health HazardOngoing
DrugJuly 18, 2014· Unique Pharmaceutical, Ltd

Recalled Item: All sterile products within expiry Recalled by Unique Pharmaceutical, Ltd...

The Issue: Lack of Sterility Assurance: A recent FDA inspection revealed poor aseptic...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2014· Unique Pharmaceutical, Ltd

Recalled Item: N-Acetyl Cysteine 20% 4 mL Vial Stock Code: 4133 Recalled by Unique...

The Issue: Non-Sterility: One lot of N-Acetyl Cysteine vials tested positive for...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 18, 2014· Smith & Nephew, Inc.

Recalled Item: RENASYS EZ/ RENASYS EZ Plus 800 mL canister with Solidifier Recalled by...

The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2014· Smith & Nephew, Inc.

Recalled Item: RENASYS EZ/ RENASYS EZ Plus 250 mL canister with Solidifier Recalled by...

The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2014· Smith & Nephew, Inc.

Recalled Item: RENASYS EZ/ RENASYS EZ Plus 800 mL canister (w/o CLP) Recalled by Smith &...

The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2014· Diagnostica Stago, Inc.

Recalled Item: Stago IVD Recalled by Diagnostica Stago, Inc. Due to Diagnostica Stago Inc....

The Issue: Diagnostica Stago Inc. received some customer complaints regarding a...

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

Class III — Low RiskOngoing
DrugJuly 17, 2014· X-Gen Pharmaceuticals Inc.

Recalled Item: Clonidine HCl Injection Recalled by X-Gen Pharmaceuticals Inc. Due to...

The Issue: Labeling: Label Error On Declared Strength: The side label description...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 17, 2014· Genesis BPS, LLC.

Recalled Item: Pedi-Pak Pedi-Syringe Filter 60 mL Becton Dickinson/Monoject Syringe Rx Only...

The Issue: Genesis BPS is recalling numerous devices since they did not notify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Genesis BPS, LLC.

Recalled Item: Pedi-Pak Pedi-Syringe Filter 35 mL Monoject Syringe Rx Only Genesis BPS...

The Issue: Genesis BPS is recalling numerous devices since they did not notify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Genesis BPS, LLC.

Recalled Item: Pedi-Pak Pedi-Syringe Filter 30 mL Becton Dickinson Syringe Rx Only Genesis...

The Issue: Genesis BPS is recalling numerous devices since they did not notify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· TomoTherapy Incorporated

Recalled Item: TomoTherapy Treatment System Recalled by TomoTherapy Incorporated Due to...

The Issue: Accuray is voluntarily recalling TomoTherapy H Series software versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Zimmer, Inc.

Recalled Item: Tapered-Screw Vent Implant Recalled by Zimmer, Inc. Due to Zimmer Dental is...

The Issue: Zimmer Dental is recalling the Tapered Screw-Vent Implant because the inner...

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

Class II — Potential Health HazardOngoing
DrugJuly 16, 2014· Bio-pharm, Inc.

Recalled Item: Rugby Children's Pain and Fever Acetaminophen Oral Suspension 160 mg/5 mL...

The Issue: Superpotent Drug: Bio-Pharm, Inc. is initiating a recall of one lot of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 16, 2014· Mars Food US

Recalled Item: Uncle Ben's(R) Ready Rice GARDEN VEGETABLE Recalled by Mars Food US Due to...

The Issue: Some pouches were filled with a different product that contains barley, a...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund