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RUSCH
TELEFLEX INCORPORATED · Model IPN044844 · UDI-DI 04026704065264
BTS
Prescription
1
510(k) clearances
2,475
Adverse events (5 deaths)
11
Recalls
11
Facilities
Description
Elbow connector
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-11-21 | Teleflex, Inc. | Customer complaints reporting that the cobb connector detached from the main connector prior to use. |
| 2014-11-21 | Teleflex, Inc. | Customer complaints reporting that the cobb connector detached from the main connector prior to use. |
| 2014-11-21 | Teleflex, Inc. | Customer complaints reporting that the cobb connector detached from the main connector prior to use. |
| 2014-11-21 | Teleflex, Inc. | Customer complaints reporting that the cobb connector detached from the main connector prior to use. |
| 2014-11-21 | Teleflex, Inc. | Customer complaints reporting that the cobb connector detached from the main connector prior to use. |
| 2014-11-21 | Teleflex, Inc. | Customer complaints reporting that the cobb connector detached from the main connector prior to use. |
| 2014-11-21 | Teleflex, Inc. | Customer complaints reporting that the cobb connector detached from the main connector prior to use. |
| 2014-11-21 | Teleflex, Inc. | Customer complaints reporting that the cobb connector detached from the main connector prior to use. |
| 2014-11-21 | Teleflex, Inc. | Customer complaints reporting that the cobb connector detached from the main connector prior to use. |
| 2014-02-28 | Teleflex Medical | The product may fail to achieve seal of right lung due to the cuff inflating to one side |
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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.