Home › Aesculap AG › SQ.LINE
SQ.LINE
Aesculap AG · Model LX184NR · UDI-DI 04046955285679
HTC
Prescription
10
510(k) clearances
412
Adverse events
4
Recalls
243
Facilities
Description
SQ.LINE Wire Extraction Pliers, tapered, 6 1/4", (160 mm), double action, pointed, ergonomic handle, double articulated joint, non-sterile, reusable
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-11-14 | The Anspach Effort, Inc. | May operate solely in reverse mode, not operate in reverse mode when intended, not function or an unintentionally start. |
| 2014-11-06 | Synthes (USA) Products LLC | The device may operate solely in reverse mode, not operate in reverse mode when intended, not function, or unintentionally start. Unintended start of the hand piece or wrong mode/ |
| 2014-08-14 | The Anspach Effort, Inc. | The affected Small Electric Drive (SED) may operate solely in reverse mode, not operate in reverse mode when intended, not function, or unintentionally start. |
| 2009-09-03 | Synthes USA (HQ), Inc. | The recalling firm has determined that the customized plates instruments do not have a cleared premarket notification. |
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.