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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Topical Products

MEDLINE INDUSTRIES INC: Vitamin A&D Ointment Recalled Due to Mislabeling

Agency Publication Date: September 12, 2017
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Summary

Medline Industries Inc. is recalling 462 cases (approximately 66,528 individual packets) of Vitamin A&D Ointment (petroleum 93.5%) because the individual foil packets inside the boxes are incorrectly labeled as petroleum jelly. While the outer boxes and cases are correctly labeled as A&D ointment, the labeling on the 0.18 oz (5g) packets themselves is wrong. This mislabeling could lead a consumer to use the product incorrectly or be unaware of the specific ingredients in the A&D formulation compared to plain petroleum jelly.

Risk

A labeling mix-up on individual packets means consumers may apply a product containing multiple ingredients when they believe they are using pure petroleum jelly. This can lead to improper treatment of skin conditions or potential allergic reactions to ingredients that were not expected based on the packet's label.

What You Should Do

  1. Check your Vitamin A&D Ointment (0.18 oz / 5g packets) for Lot Number A-K-8383 to see if your product is affected.
  2. Verify the NDC number 53329-090-16 on the outer box or case to confirm it matches the recalled product.
  3. Identify the packets by looking for individual foil packets labeled as 'petroleum jelly' that were found inside a box labeled as 'Vitamin A&D Ointment'.
  4. Contact your healthcare provider or pharmacist for guidance if you have used the mislabeled product and have concerns.
  5. Return any unused packets or boxes to the place of purchase for a refund or contact Medline Industries Inc. at 1-800-633-5463 for further instructions.
  6. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Healthcare consultation and refund

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Vitamin A&D Ointment (petroleum 93.5%), Skin Protectant (0.18 OZ / 5g)
Model:
NDC: 53329-090-16
Recall #: D-1138-2017
Lot Numbers:
A-K-8383

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 77936
Status: Resolved
Manufacturer: MEDLINE INDUSTRIES INC
Manufactured In: United States
Units Affected: 462 cases, 144 packets per case
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.