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Discount Drug Mart Food Fair

DISCOUNT DRUG MART, INC. · Model 093351031885 · UDI-DI 00093351031885

KGX
10
510(k) clearances
5,436
Adverse events (17 deaths)
48
Recalls
991
Facilities

Description

Black, Kinesiology Tape, 1 roll, 2 IN x 5.4 YDS (50 mm x 5 m), 20 Pre-Cut Strips, all one size

Recalls

DateFirmReason
2025-12-26GOLD STAR DISTRIBUTION INCPotential exposure of rodents and rodent activity in the distribution center.
2025-11-25Ferndale Laboratories, Inc.Butyrate tube cracks during actuation, rendering product unusable.
2025-10-27Medline Industries, LPMedline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
2025-10-27Medline Industries, LPMedline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
2025-10-27Medline Industries, LPMedline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
2025-10-27Medline Industries, LPMedline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
2025-10-27Medline Industries, LPMedline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
2025-10-27Medline Industries, LPMedline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
2025-10-27Medline Industries, LPMedline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
2024-04-17Cardinal Health 200, LLCPotential contamination of the product with latex adhesive residual.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.