FDA recall record

CVS Honey Pad recall — FDA Z-2512-2025

Packaging failures were identified which could lead to a breach in the sterile barrier.

Class IIclassification
Z-2512-2025official record ID
Sep 10, 2025report date

Recall record at a glance

Official recordZ-2512-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmIntegra LifeSciences Corp. (NeuroSciences)
Report dateSep 10, 2025
Recall initiation dateAug 5, 2025
Quantity111492 units
LocationPrinceton, NJ, United States

Official product description

Brand Name: CVS Honey Pad Product Name: CVS Honey Pad Model/Catalog Number: 9370613, 937404 Product Description: Infused with natural medical-grade honey Manuka (Leptospermum) honey is a medical-grade honey that is harvested from bees in New Zealand. Researchers have found that this species has unique components that make it ideal for wounds.

Why the product was recalled

Packaging failures were identified which could lead to a breach in the sterile barrier.

Distribution information

Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and the countries of Canada, Australia, New Zealand, Korea, Guam, Malaysia.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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