CLASS II Food recall · Reported 25 Dec 2013 · FDA Enforcement Report
Ut-Fem¿ For Women, urinary tract Solution recalled
Global Health Laboratories is recalling Ut-Fem¿ For Women, urinary tract Solution, Dietary Supplement, Product No. 110403, distributed in New York. The recall was initiated on 7 Nov 2013 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1105-2014
- FDA event ID
- 66765
- Recalling firm
- Global Health Laboratories, Amityville, NY
- Brand
- Ut-Fem
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 7 Nov 2013
- FDA classified
- 18 Dec 2013
- Reported
- 25 Dec 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Product category
- Dietary Supplements
Timeline
| 7 Nov 2013 | Recall initiated by company | |
| 18 Dec 2013 | Classified by FDA | +41 days |
| 25 Dec 2013 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The finished dietary supplement product was manufactured with ingredients subsequently found to be contaminated with chloramphenicol, an antibiotic, at levels above 0.3 ppb. The supplier, Specialty Enzymes & Biotechnologies, recalled the raw materials and notified the recipients. Subsequent private laboratory testing of the finished product revealed levels of chloramphenicol above 0.3 ppb.
Product as listed by the FDA
UT-Fem¿ FOR WOMEN, urinary tract SOLUTION, Dietary Supplement, 42 Vegetable Capsules, Product No. 110403, UPC 7 98304 24865 4 -- Manufactured for: Global Quality Health Inc.
Where it was distributed
New York
Questions about this recall
Why was it recalled?
The finished dietary supplement product was manufactured with ingredients subsequently found to be contaminated with chloramphenicol, an antibiotic, at levels above 0.3 ppb. The supplier, Specialty Enzymes & Biotechnologies, recalled the raw materials and notified the recipients. Subsequent private laboratory testing of the finished product revealed levels of chloramphenicol above 0.3 ppb.
Which lots are affected?
Lot Number 1256074
Where was it sold?
New York
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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