Techni-Care Surgical Hand Scrub and Patient Preoperative Skin… — Class III drug recall D-0235-2017
Terminated recall by Care-Tech Laboratories, Inc., reported 2017-01-04, distributed nationwide. Labeling: Incorrect or Missing Lot and/or Exp Date - Product is missing or has illegible lot and expiry codes,
| Recall number | D-0235-2017 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Care-Tech Laboratories, Inc., Saint Louis, MO, United States |
| Recall initiated | 2016-11-08 |
| Classified | 2016-12-23 |
| Reported by FDA | 2017-01-04 |
| Terminated | 2017-12-05 |
| Distributed | Nationwide (US) |
| Reason classes | labeling, packaging |
| NDC | 46706-0201-01, 46706-0201-02, 46706-0201-03, 46706-0201-05, 46706-0201-06 |
Product
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
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0235-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.