RecallRadar

FDA Drug recall D-1522-2012

FORMIX 100MCG / 30MG / 1MG INJECTABLE 10 ML, 10 MLS, 5 ML

On 2012-08-22 the FDA classified a Class II recall of FORMIX 100MCG / 30MG / 1MG INJECTABLE 10 ML, 10 MLS, 5 ML by Franck S Lab D B A Franck S Compounding Lab, citing lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all Sterile Human Drugs distributed between 11/21/2011 and 05/21/2012 because FDA environmental sampling re….

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1522-2012
ClassificationClass II
Statusterminated
Initiated2012-05-25
Published2012-08-22
Last updated2026-09-13 11:51 UTC
CompanyFranck S Lab D B A Franck S Compounding Lab
DistributionUS

Product

FORMIX 100MCG / 30MG / 1MG INJECTABLE 10 ML, 10 MLS, 5 ML; FORMIX 100MCG / 30MG / 2MG INJECTABLE 10 ML (4 DIFFERENT PRODUCTS)

Reason

Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all Sterile Human Drugs distributed between 11/21/2011 and 05/21/2012 because FDA environmental sampling revealed the presence of microorganisms and fungal growth in the clean room where sterile products were prepared.

Identifiers

code_infoRx #'s: 0357028 0372461 0374296 0376008 0397681 0407302 0392293 0371718 0396669

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1522-2012%22

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