Home › Peter Lazic GmbH › LAZIC
LAZIC
Peter Lazic GmbH · Model 64.516.21 · UDI-DI 04250603737889
HYA
Prescription
0
510(k) clearances
11
Adverse events (1 deaths)
1
Recalls
108
Facilities
Description
L-LINE ELLIPSE MICRO NEEDLE HOLDER BLUE CURVED, 11,0 X 0,4 MM, WITHOUT RATCHET TOTAL LENGHT 180 MM / 7", D-COATED
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-06-17 | Biomet, Inc. | Medium Bone Plate Forceps was assembled with the incorrect grip arm tip. Potential that the surgeon will be unable to provisionally clamp the plate to the patient's bone. |
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.