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. 2,531 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,531 in last 12 months

Showing 95419560 of 48,219 recalls

DrugFebruary 23, 2023· Nutraceutical Corporation

Recalled Item: NaturalCare bioAllers Recalled by Nutraceutical Corporation Due to CGMP...

The Issue: CGMP Deviations: Raw material recalled by repackager, due to discoloration.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 23, 2023· Nutraceutical Corporation

Recalled Item: NatraBio Recalled by Nutraceutical Corporation Due to CGMP Deviations: Raw...

The Issue: CGMP Deviations: Raw material recalled by repackager, due to discoloration.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 23, 2023· Nutraceutical Corporation

Recalled Item: NaturalCare Recalled by Nutraceutical Corporation Due to CGMP Deviations:...

The Issue: CGMP Deviations: Raw material recalled by repackager, due to discoloration.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 23, 2023· The Harvard Drug Group

Recalled Item: Carbidopa and Levodopa Tablets Recalled by The Harvard Drug Group Due to...

The Issue: Packaging defect: observed packaging defect, blister packaging inadequately...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 23, 2023· Aesculap Implant Systems LLC

Recalled Item: Caspar Cervical Retractor (CCR) Basket ME754 - Lid Only and Recalled by...

The Issue: Mislabeled: Product is marked with GTIN # 04046955299592 however; the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2023· Olympus Corporation of the Americas

Recalled Item: Single Use Rotatable Clip Fixing Device Model HX 201LR 135 - Rotatable...

The Issue: There have been complaints that the clip did not come out of the tube sheath...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2023· Remote Diagnostic Technologies Ltd.

Recalled Item: Tempus Pro Patient Monitor is a portable vital signs monitor Recalled by...

The Issue: During internal testing, Regulatory Compliance issues were identified...

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

Class II — Potential Health HazardOngoing
DrugFebruary 22, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Norepinephrine Bitartrate in 0.9% Sodium Chloride Injection Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Phenylephrine HCl Injection Recalled by Nephron Sterile Compounding Center...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Phenylephrine HCl in 0.9% Sodium Chloride Injection Recalled by Nephron...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Diltiazem HCl in 0.7% Sodium Chloride Injection Recalled by Nephron Sterile...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Phenylephrine HCl Injection Recalled by Nephron Sterile Compounding Center...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Norepinephrine Bitartrate in 0.9% Sodium Chloride Injection Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Norepinephrine Bitartrate in 0.9% Sodium Chloride Injection Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Phenylephrine HCl Injection Recalled by Nephron Sterile Compounding Center...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 21, 2023· Padagis US LLC

Recalled Item: Evamist (estradiol transdermal spray) Recalled by Padagis US LLC Due to...

The Issue: Failed Content Uniformity Specifications: The Spray Content Uniformity (SCU)...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 21, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Phenylephrine HCl 40 mg (160 mcg/mL) added to 0.9% Sodium Chloride 250 mL IV...

The Issue: CGMP DEVIATIONS

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 21, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Phenylephrine HCl 0.5 mg per 5 mL (100 mcg/mL) Recalled by Denver Solutions,...

The Issue: CGMP DEVIATIONS

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 21, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Phenylephrine HCl 1mg per 10mL (100 mcg/mL) 10 mL syringes Recalled by...

The Issue: CGMP DEVIATIONS

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 21, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Phenylephrine HCl 20 mg (80 mcg/mL) added to 0.9% Sodium Chloride 250 mL IV...

The Issue: CGMP DEVIATIONS

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

Class II — Potential Health HazardOngoing
Refund