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. 2,348 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,348 in last 12 months

Showing 3506135080 of 48,219 recalls

DrugSeptember 3, 2015· Kalman Health & Wellness, Inc. dba Essential Wellness Pharma

Recalled Item: HCG 3000 Units/mL Injection Recalled by Kalman Health & Wellness, Inc. dba...

The Issue: Lack of Assurance of Sterility: A recall of all compounded sterile...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2015· Kalman Health & Wellness, Inc. dba Essential Wellness Pharma

Recalled Item: 17-Alpha Hydroxyprogesterone 250 mg/mL in Castor Oil Injection Recalled by...

The Issue: Lack of Assurance of Sterility: A recall of all compounded sterile...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2015· Kalman Health & Wellness, Inc. dba Essential Wellness Pharma

Recalled Item: TRIMIX #1 Injection Recalled by Kalman Health & Wellness, Inc. dba Essential...

The Issue: Lack of Assurance of Sterility: A recall of all compounded sterile...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2015· Kalman Health & Wellness, Inc. dba Essential Wellness Pharma

Recalled Item: Progesterone 100 mg/mL Ethyl Oleate Injection Recalled by Kalman Health &...

The Issue: Lack of Assurance of Sterility: A recall of all compounded sterile...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 3, 2015· Bausch & Lomb Inc Irb

Recalled Item: BAUSCH + LOMB Biotrue ONEday lenses (nesofilcon A) Recalled by Bausch & Lomb...

The Issue: The firm determined that 25 lots had been manufactured with a minor surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2015· Steris Corporation

Recalled Item: AMSCO 400 and AMSCO C Small Steam Sterilizers Recalled by Steris Corporation...

The Issue: In AMSCO Small Steam Sterilizers equipped with the CS-iQ feature, the...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 3, 2015· Synthes (USA) Products LLC

Recalled Item: Inserter for Titanium Elastic Nails (TEN) Recalled by Synthes (USA) Products...

The Issue: potential for mechanical failures such as breakage.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2015· Leica Microsystems, Inc.

Recalled Item: Novocastra Lyophilized Mouse Monoclonal Antibody CD10 (CD10)....

The Issue: These Lot numbers are not stable up to the expiry date on the product labeling.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2015· Zimmer Gmbh

Recalled Item: Zimmer Natural Nail CM Long. Intramedullary Fixation Rod. The Zimmer...

The Issue: In about 5% of tested samples, the outer tray was found to be compromised....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas b 123 POC system The cobas b 123 POC Recalled by Roche Diagnostics...

The Issue: under specific settings, an issue may occur during simultaneous Sensor...

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

Class II — Potential Health HazardOngoing
DrugSeptember 2, 2015· Baxter Healthcare Corporation

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corporation Due...

The Issue: Lack of Assurance of Sterility: Recalling firm reported a complaint for mold...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 2, 2015· Sincerely Nuts

Recalled Item: Sincerely Nuts brand Macadamia Nuts (Raw) (a) Whole Recalled by Sincerely...

The Issue: Raw Macadamia Nuts were found to be contaminated with Salmonella based on...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 1, 2015· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic CryoConsole Recalled by Medtronic Inc. Cardiac Rhythm Disease...

The Issue: An issue with a USB memory component contained within a subset of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iTotal CR (Cruciate Retaining) Knee Replacement System-iTOTAL CR...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iUni Unicondylar Knee Replacement System: iUNI G2 Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConFormis iTotal CR Knee Replacement System- iTOTAL CR Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iUni Unicondylar Knee Replacement System- iUNI G2 Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iUNI Unicondylar Knee Replacement System iUNI G2 Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...

The Issue: When performing head or neck scans, the currently displayed SAR values could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...

The Issue: When performing head or neck scans, the currently displayed SAR values could...

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

Class II — Potential Health HazardOngoing