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Class II: temporary or reversible health riskOngoing

A-S Medication Solutions Valsartan Tablets Recall

Valsartan Tablets, 80 MG, 30-count bottle (NDC 54569-6582-0, 90-count bottle (NDC 54569…

A-S Medication Solutions LLC. · Libertyville, IL

Risk level
Class II
Reported by FDA
Aug 29, 2018
Recall ID
D-1109-2018
Check your lot numberHow we source this data

Summary

A-S Medication Solutions recalled Valsartan Tablets starting Jul 17, 2018. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1109-2018 on Aug 29, 2018. Reason: CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product. Status: Ongoing.

Why it was recalled

CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

Product description

Valsartan Tablets, 80 MG, 30-count bottle (NDC 54569-6582-0, 90-count bottle (NDC 54569-6582-1), Rx Only, MFG: Zhejiang Huahai Pharma, Linhai, Zhejiang 317024 China

Lot numbers, UPCs & expiration codes

Expiry, lot: [30-count] 11/30/2018: 7258177, 7276228; 2/28/2019: 7212260; [90-count] 11/30/2018: 7208140; 2/28/2019: 7212261, 7221155, 7222161; 8/31/2019: 8109171; 9/30/2019: 8109170

Where it was sold

Nationwide USA

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-1109-2018
Classification
Class II
Status
Ongoing
Recall initiated
Jul 17, 2018
FDA report date
Aug 29, 2018
Quantity
178 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
A-S Medication Solutions LLC.

Original FDA data

Every field from FDA enforcement report D-1109-2018, exactly as published.

Show all FDA fields
City
Libertyville
State
IL
Status
Ongoing
Country
United States
Event ID
80748
Address
2401 Commerce Dr
Code information
Expiry, lot: [30-count] 11/30/2018: 7258177, 7276228; 2/28/2019: 7212260; [90-count] 11/30/2018: 7208140; 2/28/2019: 7212261, 7221155, 7222161; 8/31/2019: 8109171; 9/30/2019: 8109170
Postal code
60048-4464
Report date
Aug 29, 2018
Product type
Drugs
Recall number
D-1109-2018
Classification
Class II
Recalling firm
A-S Medication Solutions LLC.
Product quantity
178 bottles
Reason for recall
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Valsartan Tablets, 80 MG, 30-count bottle (NDC 54569-6582-0, 90-count bottle (NDC 54569-6582-1), Rx Only, MFG: Zhejiang Huahai Pharma, Linhai, Zhejiang 317024 China
Distribution pattern
Nationwide USA
Recall initiation date
Jul 17, 2018
Initial firm notification
Letter
Center classification date
Aug 18, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1109-2018, published Aug 29, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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