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Class II: temporary or reversible health riskTerminated

Isomeric Pharmacy Solution Methylprednisolone Acetate 40 mg/mL Recall

Methylprednisolone Acetate 40 mg/mL, Lidocaine HCl 10 mg/mL, 10 mL Multi-Dose Vial For…

Isomeric Pharmacy Solution, LLC · Salt Lake City, UT

Risk level
Class II
Reported by FDA
May 3, 2017
Recall ID
D-0681-2017
Check your lot numberHow we source this data

Summary

Isomeric Pharmacy Solution recalled Methylprednisolone Acetate 40 mg/mL starting Apr 6, 2017. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0681-2017 on May 3, 2017. Reason: Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile. Status: Terminated.

Why it was recalled

Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Product description

Methylprednisolone Acetate 40 mg/mL, Lidocaine HCl 10 mg/mL, 10 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Drive, SLC, UT 84109, Part # 1010, barcode 3 70285 10101 4.

Lot numbers, UPCs & expiration codes

Lot #s: 09007, Exp 04/04/17; 09016, Exp 04/16/17; 09020, Exp 04/18/17; 09025, Exp 04/23/17; 10026, 10030, Exp 05/28/17; 11007, Exp 05/30/17; 11008, Exp 05/31/17; 11020, Exp 06/07/17; 11028, Exp 06/12/17; 11043, Exp 06/26/17.

Where it was sold

Nationwide in the USA and Puerto Rico

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-0681-2017
Classification
Class II
Status
Terminated
Recall initiated
Apr 6, 2017
FDA report date
May 3, 2017
Quantity
4,001 vials
Recall type
Voluntary: Firm initiated
Recalling firm
Isomeric Pharmacy Solution, LLC

Original FDA data

Every field from FDA enforcement report D-0681-2017, exactly as published.

Show all FDA fields
City
Salt Lake City
State
UT
Status
Terminated
Country
United States
Event ID
76951
Address
2401 S Foothill Dr Ste D
Code information
Lot #s: 09007, Exp 04/04/17; 09016, Exp 04/16/17; 09020, Exp 04/18/17; 09025, Exp 04/23/17; 10026, 10030, Exp 05/28/17; 11007, Exp 05/30/17; 11008, Exp 05/31/17; 11020, Exp 06/07/17; 11028, Exp 06/12/17; 11043, Exp 06/26/17.
Postal code
84109-1479
Report date
May 3, 2017
Product type
Drugs
Recall number
D-0681-2017
Classification
Class II
Recalling firm
Isomeric Pharmacy Solution, LLC
Product quantity
4,001 vials
Termination date
Aug 30, 2017
Reason for recall
Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Methylprednisolone Acetate 40 mg/mL, Lidocaine HCl 10 mg/mL, 10 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Drive, SLC, UT 84109, Part # 1010, barcode 3 70285 10101 4.
Distribution pattern
Nationwide in the USA and Puerto Rico
Recall initiation date
Apr 6, 2017
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Apr 26, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0681-2017, published May 3, 2017. View the source record (openFDA) · FDA enforcement reports

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

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