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DARCO® Body Armor® Elastic Tape, strong (light blue)

DARCO INTERNATIONAL, INC. · Model BAET-LB · UDI-DI 00609271629912

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

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.