US Drug Recall Register
Class III · Low risk Terminated Initiated Nov 8, 2016 (10 years ago)

Techni-Care Surgical Hand Scrub and Patient Preoperative Skin Preparation (3.0% w/v…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Labeling: Incorrect or Missing Lot and/or Exp Date - Product is missing or has illegible lot and expiry codes, as well as defective or cracked caps.

What was recalled

Techni-Care Surgical Hand Scrub and Patient Preoperative Skin Preparation (3.0% w/v Chloroxylenol), packaged in a) 4 oz. bottles (NDC 46706-201-01), b) 8 oz bottles (NDC 46706-201-02), c) 16 oz. bottles (NDC 46706-201-03), d) 12 oz. pumpette (NDC 46706-201-05), e) 32 oz. bottles (NDC 46706-201-06), OTC, Care-Tech Laboratories, Inc., St. Louis, MO 63139

Recalling firm
Care-Tech Laboratories, Inc.
NDC code
46706-201-01
Origin
MO, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0235-2017

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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