Severity
Moderate
ModerateClass IITerminated
FDA Drug recall · Reported September 16, 2015
Surgicept (Ethyl alcohol 70% w/w) WATERLESS Surgical Hand Scrub & Healthcare Personnel Handwash in 1150 mL bottles. MARKETED BY: CafeFusion, Leawood, KS 66211, MANUFACTURED FOR: HEALTHPOINT, LTD Ft. Worth, Texas 76107, MANUFACTURED BY: DPT LABORATORIES, LTD 3300 Research Plaza Brooks City-Base, Texas 78235. NDC: 0064-1080-11
Chemical Contamination: Naphthalene compound identified in the product after complaints of a petroleum odor.
Healthpoint, Ltd recalled Surgicept (Ethyl alcohol 70% w/w) WATERLESS Surgical Hand Scrub & Healthcare Personnel Ha… - a moderate-severity action.
Surgicept (Ethyl alcohol 70% w/w) WATERLESS Surgical Hand Scrub & Healthcare Personnel Ha… was recalled by Healthpoint, Ltd in September 16, 2015. Reason: Chemical Contamination: Naphthalene compound identified in the product after complaints of a petroleum odor.. Check the official notice for the remedy. Verify recall #D-1427-2015 with the FDA Drug before acting.
The recall
Healthpoint, Ltd issued this moderate-severity FDA Drug recall-Chemical Contamination: Naphthalene compound identified in the product after complaints of a petroleum odor..
- Moderate
- severity level
- Class II
- classification
- September 16, 2015
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-1427-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-1427-2015) was formally reported on September 16, 2015, with the manufacturer initiating the action on September 4, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. Healthpoint, Ltd is listed as the recalling firm, operating out of Fort Worth, TX. Federal records list the affected scope as 11,910 bottles.
The documented reason for this recall is: Chemical Contamination: Naphthalene compound identified in the product after complaints of a petroleum odor. Distribution data in the federal record shows the product reached: Nationwide. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
11,910 bottles
Related Recalls
6
0 from same agency
Product description
Surgicept (Ethyl alcohol 70% w/w) WATERLESS Surgical Hand Scrub & Healthcare Personnel Handwash in 1150 mL bottles. MARKETED BY: CafeFusion, Leawood, KS 66211, MANUFACTURED FOR: HEALTHPOINT, LTD Ft. Worth, Texas 76107, MANUFACTURED BY: DPT LABORATORIES, LTD 3300 Research Plaza Brooks City-Base, Texas 78235. NDC: 0064-1080-11
Reason for recall
Chemical Contamination: Naphthalene compound identified in the product after complaints of a petroleum odor.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-1427-2015 |
| Date reported | September 16, 2015 |
| Date initiated | September 4, 2015 |
| Recalling firm | Healthpoint, Ltd |
| Firm location | Fort Worth, TX |
| Affected scope | 11,910 bottles |
| Distribution | Nationwide |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-1427-2015) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Surgicept (Ethyl alcohol 70% w/w) WATERLESS Surgical Hand Scrub & Healthcare Personnel Handwash in 1150 mL bottles. MARKETED BY: CafeFusion, Leawood, KS 66211, MANUFACTURED FOR: HEALTHPOINT, LTD Ft. Worth, Texas 76107, MANUFACTURED BY: DPT LABORATORIES, LTD 3300 Research Plaza Brooks City-Base, Texas 78235. NDC: 0064-1080-11. Recalled by Healthpoint, Ltd. Units affected: 11,910 bottles.
Why was this product recalled? ▼
Chemical Contamination: Naphthalene compound identified in the product after complaints of a petroleum odor.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on September 16, 2015. Severity: Moderate. Recall number: D-1427-2015.
Where was the recalled product distributed? ▼
Distribution: Nationwide.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-1427-2015) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported September 16, 2015. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.