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Lower risk Drug recall · FDA · Published November 8, 2016

Care-Tech Techni-Care Surgical Hand Scrub: Missing Lot/Exp Dates Risk

Care-Tech recalls Techni-Care Surgical Hand Scrub products with missing or illegible lot and expiration dates, which could lead to improper use. Affected items include 4oz, 8oz, 16oz bottles and 12oz pumpette with specific lot numbers and expiration dates.

🇺🇸 FDA recall #D-0235-2017DrugCare-Tech ›
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Recalling firmCare-Tech Laboratories, Inc.3224 S Kingshighway Blvd · Saint Louis, MO 63139-1114
✎ GovInfoNow plain-language explainer

What happened, in plain English

Care-Tech is recalling Techni-Care Surgical Hand Scrub products that have missing or illegible lot and expiration dates. This could lead to improper use if the product's age or batch is not known, potentially causing safety issues in medical settings. Read more at govinfonow.com/recall/42258-care-tech-techni-care-surgical-hand-scrub-missing-lot-exp.

Source Summary by GovInfoNow · govinfonow.com/recall/42258-care-tech-techni-care-surgical-hand-scrub-missing-lot-exp · Updated October 8, 2026 · FDA enforcement record: FDA #D-0235-2017

Cite this page

“Care-Tech Techni-Care Surgical Hand Scrub: Missing Lot/Exp Dates Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/42258-care-tech-techni-care-surgical-hand-scrub-missing-lot-exp. Based on FDA recall #D-0235-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0235-2017%22&limit=1).

Why it’s dangerous

The products lack clear lot and expiration codes, making it impossible to verify their age or batch. This could lead to using expired or incorrect products, which might not be safe for medical procedures.

Who’s affected

Healthcare workers and patients using the Techni-Care Surgical Hand Scrub products with missing or illegible lot and expiration dates. Those handling the products without knowing the correct batch or expiration could be at risk.

How to tell if you have this one

Check for missing or illegible lot and expiration codes on the bottle. Affected products include 4oz, 8oz, 16oz bottles and 12oz pumpette with specific lot numbers and expiration dates listed in the recall notice.

  • Brand
    Care-Tech
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Labels

    Look for missing or illegible lot and expiration codes on the bottle.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 13 months after the firm started it.

1. Firm started the recall: Nov 8, 201612. FDA classified it Class III: Dec 23, 201623. Published in FDA’s Enforcement Report: Jan 4, 201734. FDA terminated the recall: Dec 5, 2017420162017
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0235-2017 (November 8, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0235-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA