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Class II: temporary or reversible health riskTerminated

Isomeric Pharmacy Solution Phenylephrine 2 Recall

Phenylephrine 2

Isomeric Pharmacy Solution, LLC · Salt Lake City, UT

Risk level
Class II
Reported by FDA
May 3, 2017
Recall ID
D-0687-2017
Check your lot numberHow we source this data

Summary

Isomeric Pharmacy Solution recalled Phenylephrine 2 starting Apr 6, 2017. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0687-2017 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

Phenylephrine 2.5%, Tropicamide 1%, 15 mL Multi-Dose Ophthalmic (spelled Opthalmic) Drops in a bottle, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1300, barcode 3 70285 13001 4.

Lot numbers, UPCs & expiration codes

Lot Numbers: 10003, Exp 04/05/17; 10018, Exp 04/17/17; 10023, Exp 04/23/17; 10025, Exp 04/24/17; 10027, Exp 04/29/17; 11011, 11012, Exp 05/07/17; 11024, 11026, Exp 05/14/17; 11029, Exp 05/16/17; 11030, Exp 05/17/17; 11032, Exp 05/21/17; 11045, Exp 06/04/17; 12008, Exp 06/13/17; 12014, 12015, Exp 06/20/17; 12022, 12024, Exp 06/28/17; 13001, 13002, Exp 07/03/17; 13011, 13012, Exp 07/09/17.

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-0687-2017
Classification
Class II
Status
Terminated
Recall initiated
Apr 6, 2017
FDA report date
May 3, 2017
Quantity
5,165 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Isomeric Pharmacy Solution, LLC

Original FDA data

Every field from FDA enforcement report D-0687-2017, 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 Numbers: 10003, Exp 04/05/17; 10018, Exp 04/17/17; 10023, Exp 04/23/17; 10025, Exp 04/24/17; 10027, Exp 04/29/17; 11011, 11012, Exp 05/07/17; 11024, 11026, Exp 05/14/17; 11029, Exp 05/16/17; 11030, Exp 05/17/17; 11032, Exp 05/21/17; 11045, Exp 06/04/17; 12008, Exp 06/13/17; 12014, 12015, Exp 06/20/17; 12022, 12024, Exp 06/28/17; 13001, 13002, Exp 07/03/17; 13011, 13012, Exp 07/09/17.
Postal code
84109-1479
Report date
May 3, 2017
Product type
Drugs
Recall number
D-0687-2017
Classification
Class II
Recalling firm
Isomeric Pharmacy Solution, LLC
Product quantity
5,165 bottles
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
Phenylephrine 2.5%, Tropicamide 1%, 15 mL Multi-Dose Ophthalmic (spelled Opthalmic) Drops in a bottle, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1300, barcode 3 70285 13001 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-0687-2017, published May 3, 2017. View the source record (openFDA) · FDA enforcement reports

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

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