Home › TIDI PRODUCTS, LLC › Grip-Lok
Grip-Lok
TIDI PRODUCTS, LLC · Model 2100NOCH · UDI-DI 00618125191208
10
510(k) clearances
1,812
Adverse events (30 deaths)
6
Recalls
267
Facilities
Description
Nasal Oxygen Cannula Hydrocolloid Securement Device For lines and tubes sized 4.5 - 19 Fr
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-07-06 | Smiths Medical ASD Inc. | "Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured. |
| 2018-07-06 | Smiths Medical ASD Inc. | "Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured. |
| 2018-07-06 | Smiths Medical ASD Inc. | "Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured. |
| 2018-07-06 | Smiths Medical ASD Inc. | "Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured. |
| 2018-07-06 | Smiths Medical ASD Inc. | "Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured. |
| 2017-05-09 | Teleflex Medical | Incorrect labeling; the box label indicates Pediatric, the product insert indicates an Adult device. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.