Home › Spiggle & Theis Medizintechnik GmbH › Aluminium Ext. Nasal Splints,
Aluminium Ext. Nasal Splints,
Spiggle & Theis Medizintechnik GmbH · Model 72-3022 BT · UDI-DI 04250381823682
EPP
Prescription
10
510(k) clearances
19
Adverse events
2
Recalls
38
Facilities
Description
66x45x42 mm, large, self-adh. back,(like 2060400) 25/box
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-02-21 | Medtronic Xomed, Inc. | Medtronic Xomed, Inc. Jacksonville, FL issued a recall on Feb 21, 2011 for all lots of the alcohol pad packaged with the Medtronic's External Nasal Splints REF 1528116 (sm), 152812 |
| 2011-02-21 | Medtronic Xomed, Inc. | Medtronic Xomed, Inc. Jacksonville, FL issued a recall on Feb 21, 2011 for all lots of the alcohol pad packaged with the Medtronic's External Nasal Splints REF 1528116 (sm), 152812 |
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.
