Reported Aug 22, 2012 · Terminated

LEUCOVORIN, LYOPHILIZED 100 MG VIAL INJECTABLE 1 VIAL 10 VIAL 100 VIAL 2 VIAL 24 VIAL 30 VIAL 50 VIAL 60 VIAL 76 VIAL;…

Franck's Lab Inc., d.b.a. Franck's Compounding Lab

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Franck's Lab Inc., d.b.a. Franck's Compounding Lab · 1210 SW 33rd Avenue · Ocala, FL · 34474-5138

Is this the product you have?

  • LEUCOVORIN, LYOPHILIZED 100 MG VIAL INJECTABLE 1 VIAL 10 VIAL 100 VIAL 2 VIAL 24 VIAL 30 VIAL 50 VIAL 60 VIAL 76 VIAL; LEUCOVORIN, LYOPHILIZED 350 MG VIAL INJECTABLE 10 VIAL 15 VIAL 20 VIAL 22 VIAL 28 VIAL 30 VIAL 4 VIAL 40 VIAL 5 VIAL 50 VIAL 8 VIAL; LEUCOVORIN, LYOPHILIZED 500 MG VIAL INJECTABLE 10 VIAL 14 VIAL 15 VIAL 17 VIAL 2 VIAL 20 VIAL 23 VIAL 25 VIAL 27 VIAL 3 VIAL 30 VIAL 33 VIAL 36 VIAL 5 VIAL 50 VIAL (35 DIFFERENT PRODUCTS)
Lot codes and dates
  • Rx #'s:
    • 0403290
    • 0405427
    • 0382085
    • 0403290
    • 0382085
    • 0405142
    • 0391560
    • 0391560
    • 0382085
    • 0362356
    • 0362504
    • 0376747
    • 0398606
    • 0405426
    • 0362504
    • 0362504
    • 0376747
    • 0402778
    • 0405426
    • 0395599
    • 0395599
    • 0405112
    • 0406366
    • 0388985
    • 0391567
    • 0396672
    • 0405426
    • 0395599
    • 0398606
    • 0360280
    • 0385032
    • 0390726
    • 0402210
    • 0398232
    • 0360280
    • 0362394
    • 0393068
    • 0403288
    • 0360025
    • 0369905
    • 0379934
    • 0393068
    • 0402985
    • 0403256
    • 0399150
    • 0360025
    • 0372389
    • 0399150
    • 0402985
    • 0399150
    • 0403288
    • 0372389
    • 0393068
    • 0398232
    • 0360280
    • 0362394
    • 0393068
    • 0398232
Amount recalled
72 units

This recall covers 198 products

The agency filed one notice per product. You are reading one of them; the other 197 are below.

185 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

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. FDA environmental sampling revealed the presence of microorganisms and fungal growth in the clean room where sterile products were prepared.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Aug 15, 2014 · Data as of Sep 19, 6:29 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.