FindMyRecallSubscribe
Class II: temporary or reversible health riskTerminated

ImprimisRx CA, Inc., dba ImprimisRx Timolol-Brimonidine-Dorzolamide-Latanoprost Recall

Timolol-Brimonidine-Dorzolamide-Latanoprost (0

ImprimisRx CA, Inc., dba ImprimisRx · Irvine, CA

Risk level
Class II
Reported by FDA
Sep 13, 2017
Recall ID
D-1133-2017
Check your lot numberHow we source this data

Summary

ImprimisRx CA, Inc., dba ImprimisRx recalled Timolol-Brimonidine-Dorzolamide-Latanoprost starting Jun 23, 2017. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1133-2017 on Sep 13, 2017. Reason: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier. Status: Terminated.

Why it was recalled

Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier

Product description

Timolol-Brimonidine-Dorzolamide-Latanoprost (0.5/0.15/2/0.005)% Ophthalmic Drops, Sterile 5ml Bottle, Compounded for a licensed professional or patient use, imprimisRx, Irvine, CA

Lot numbers, UPCs & expiration codes

05092017@2B, 11/5/2017

Where it was sold

Nationwide

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-1133-2017
Classification
Class II
Status
Terminated
Recall initiated
Jun 23, 2017
FDA report date
Sep 13, 2017
Quantity
2 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
ImprimisRx CA, Inc., dba ImprimisRx

Original FDA data

Every field from FDA enforcement report D-1133-2017, exactly as published.

Show all FDA fields
City
Irvine
State
CA
Status
Terminated
Country
United States
Event ID
77647
Address
9257 Research Dr
Code information
05092017@2B, 11/5/2017
Postal code
92618-4286
Report date
Sep 13, 2017
Product type
Drugs
Recall number
D-1133-2017
Classification
Class II
Recalling firm
ImprimisRx CA, Inc., dba ImprimisRx
Product quantity
2 bottles
Termination date
Jan 14, 2019
Reason for recall
Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier
Voluntary / mandated
Voluntary: Firm initiated
Product description
Timolol-Brimonidine-Dorzolamide-Latanoprost (0.5/0.15/2/0.005)% Ophthalmic Drops, Sterile 5ml Bottle, Compounded for a licensed professional or patient use, imprimisRx, Irvine, CA
Distribution pattern
Nationwide
Recall initiation date
Jun 23, 2017
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Sep 7, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1133-2017, published Sep 13, 2017. 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.

How we source and update recall data · Report incorrect information

Other recent drug recalls