HIGHFDA DRUG

Dynarex Obstetrical Towelettes Cleanser Recall 2026 for CGMP Deviations

Dynarex Obstetrical Towelettes Cleanser is under an active FDA recall as of Jan. 20, 2026. The recall cites CGMP Deviations that could affect product quality. Consumers and healthcare providers should stop using the product immediately and contact ACME United Corporation or a healthcare provider for guidance.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
January 20, 2026
Status
ACTIVE
Severity
6/10

Quick Facts at a Glance

Recall Date
January 20, 2026
Hazard Level
HIGH
Brands
BZK PADS, Dynarex Corporation
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL, PREGNANT

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
BZK PADS, Dynarex Corporation
Product type
Obstetrical Towelettes Cleanser (BZK Towelettes)
Model numbers
Lot #: 52347-R, 52348-R, 52349-R, 52350-R, 52351-R, 52352-R, 53518, 53519 +1 more
UPC codes
67777-244, 67777-244-02, 67777-244-01
Sizes
5" x 7"
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    January 20, 2026

  2. Reported by FDA DRUG

    March 11, 2026

  3. RecallRadar source check

    March 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

CGMP Deviations

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact ACME UNITED CORPORATION or your healthcare provider for guidance. Notification method: Letter

About This Product

Obstetrical Towelettes Cleanser are disposable wipes used in obstetric settings or personal care for cleansing. The product is marketed under the brand BZK PADS and manufactured for Dynarex Corporation.

Why This Is Dangerous

CGMP Deviations suggest manufacturing quality-control issues that could affect product safety or efficacy.

Industry Context

This recall is not described as part of a broader industry pattern in the notice.

Real-World Impact

Consumers and healthcare providers should avoid use until further guidance is issued. No injuries are reported in the notice, but high-risk labeling warrants caution.

Practical Guidance

How to identify if yours is affected

  1. Look for Exp. Date Mar 2027.

Where to find product info

FDA enforcement page for recall D-0369-2026 (URL provided in notice).

What timeline to expect

Remedy timeline not specified in recall notice.

If the manufacturer is unresponsive

  • Escalate to FDA at the recall page.
  • Consult your healthcare provider for guidance on safe alternatives.

How to prevent similar issues

  • Verify CGMP compliance if purchasing medical wipes.
  • Check NDC codes and expiration dates before use.
  • Monitor recalls.gov or FDA page for updates on this product category.

Documentation advice

Keep the recall notice, lot numbers, expiration dates, and any communications with ACME United Corporation for records.

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Product Details

NDC: 67777-244-02. Lot numbers: 52347-R, 52348-R, 52349-R, 52350-R, 52351-R, 52352-R, 53518, 53519. Exp. Date: Mar 2027. Size: 5" x 7". Sold nationwide in the United States. Manufacturer: Dynarex Corporation, 10 Glenshaw Street, Orangeburg, NY 10962, USA. Made in USA. Distribution: Nationwide within the United States.

Key Facts

  • Recall number D-0369-2026
  • Brand: BZK PADS; Manufacturer: Dynarex Corporation
  • Hazard: CGMP Deviations; High risk
  • Lot numbers include 52347-R through 52352-R and 53518, 53519
  • Exp. Date: Mar 2027
  • Sold nationwide in the U.S.

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
6/ 10
Affected Groups
GENERALPREGNANT
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
Lot #: 52347-R
52348-R
52349-R
52350-R
52351-R
+4 more
UPC Codes
67777-244
67777-244-02
67777-244-01
Affected States
ALL
Report Date
March 11, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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