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Dexcom G7 AR Overlay 10-Pack
Dexcom, Inc. · Model MT-1000564 · UDI-DI 00386270000415
1
510(k) clearances
5,063
Adverse events (16 deaths)
48
Recalls
985
Facilities
Description
G7 AR Overlay 10-Pack
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.