Home › TELEFLEX INCORPORATED › RUSCH
RUSCH
TELEFLEX INCORPORATED · Model IPN052734 · UDI-DI 04026704306206
GBA
Prescription
5
510(k) clearances
756
Adverse events (55 deaths)
1
Recalls
37
Facilities
Description
Word Catheter, Sterile
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-05-31 | Karl Storz Endoscopy America Inc | Karl Storz Endoscopy-America has initiated the recall of the 27023WU Balloon Catheter because the packaging may be compromised, and therefore the sterility of the product could be |
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.