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. 2,503 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,503 in last 12 months

Showing 1330113320 of 48,219 recalls

DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Vancomycin HCl Recalled by Edge Pharma, LLC Due to Lack of Assurance of...

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
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Lidocaine HCL / Bupivacaine HCL (contains Hyaluronidase 15 units/mL)...

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
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: PHENYLephrine Recalled by Edge Pharma, LLC Due to Lack of Assurance of Sterility

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
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Trypan Blue 0.03% Recalled by Edge Pharma, LLC Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: LT Topical Cream Recalled by Edge Pharma, LLC Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Lidocaine HCl/Phenylephrine HCl Nasal Solution Recalled by Edge Pharma, LLC...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Vancomycin HCl in 0.9 % Sodium Chloride Injection Recalled by Edge Pharma,...

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
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Ceftazidime Recalled by Edge Pharma, LLC Due to Lack of Assurance of Sterility

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
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: CSF Otic Insufflation Capsule Recalled by Edge Pharma, LLC Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Methotrexate Recalled by Edge Pharma, LLC Due to Lack of Assurance of Sterility

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
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Tetracaine HCl Nasal Solution Recalled by Edge Pharma, LLC Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Phenylephrine HCl Recalled by Edge Pharma, LLC Due to Lack of Assurance of...

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
DrugDecember 6, 2021· Medique Products

Recalled Item: Physicians CARE Extra Strength PAIN RELIEVER [Acetaminophen Recalled by...

The Issue: CGMP Deviations: manufacturer recalled after an FDA inspection noted that...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Medique Products

Recalled Item: Extra Strength Headache (acetaminophen 250 mg Recalled by Medique Products...

The Issue: CGMP Deviations: manufacturer recalled after an FDA inspection noted that...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Medique Products

Recalled Item: Medique Pain-Off (Acetaminophen 250 mg Recalled by Medique Products Due to...

The Issue: CGMP Deviations: manufacturer recalled after an FDA inspection noted that...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Valisa MFG LLC

Recalled Item: kleantouch HAND SANITIZER (ethyl alcohol 70%) Recalled by Valisa MFG LLC Due...

The Issue: Marketed Without an Approved NDA/ANDA: Product labeled to contain methanol...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 6, 2021· ev3 Inc.

Recalled Item: Medtronic HawkOne Directional Atherectomy System Recalled by ev3 Inc. Due to...

The Issue: Reports have been received of tip damage during use of the devices which...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 6, 2021· ev3 Inc.

Recalled Item: Medtronic HawkOne Directional Atherectomy System Recalled by ev3 Inc. Due to...

The Issue: Reports have been received of tip damage during use of the devices which...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 6, 2021· Abbott Molecular, Inc.

Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to There is a...

The Issue: There is a potential for abnormal (non-sigmoidal) amplification curves.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2021· Abbott Molecular, Inc.

Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to There is a...

The Issue: There is a software issue associated with the ability to properly complete a...

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

Class II — Potential Health HazardOngoing