Home › TELEFLEX INCORPORATED › RUSCH
RUSCH
TELEFLEX INCORPORATED · Model IPN045268 · UDI-DI 04026704553754
MGP
Prescription
1
510(k) clearances
95
Adverse events (1 deaths)
1
Recalls
22
Facilities
Description
ASHERMAN CHEST SEAL BULK
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-02-11 | Hartmann USA, Inc | Misbranded; the expiry date on the primary packing incorrectly indicates 2010-10, instead of 2015-10. Consignees were notified by letter on/about 02/11/2011. They were advised to e |
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.