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Tensoplast
BSN MEDICAL (PTY) LTD · Model 72050-57 · UDI-DI 04042809019308
10
510(k) clearances
4,983
Adverse events (15 deaths)
48
Recalls
983
Facilities
Description
TENSOPLAST 5CM X 1.5M 6 BLOWN
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-12-26 | GOLD STAR DISTRIBUTION INC | Potential exposure of rodents and rodent activity in the distribution center. |
| 2025-11-25 | Ferndale Laboratories, Inc. | Butyrate tube cracks during actuation, rendering product unusable. |
| 2025-10-27 | Medline Industries, LP | Medline 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. |
| 2025-10-27 | Medline Industries, LP | Medline 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. |
| 2025-10-27 | Medline Industries, LP | Medline 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. |
| 2025-10-27 | Medline Industries, LP | Medline 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. |
| 2025-10-27 | Medline Industries, LP | Medline 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. |
| 2025-10-27 | Medline Industries, LP | Medline 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. |
| 2025-10-27 | Medline Industries, LP | Medline 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. |
| 2024-04-17 | Cardinal Health 200, LLC | Potential contamination of the product with latex adhesive residual. |
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Get your free API keyRead the docsData 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.