Home › ASPEN SURGICAL PRODUCTS, INC. › Symmetry Jackson
Symmetry Jackson
ASPEN SURGICAL PRODUCTS, INC. · Model 74-5715E · UDI-DI 00887482124338
KAE
Prescription
10
510(k) clearances
82
Adverse events
1
Recalls
224
Facilities
Description
Symmetry® Forceps, Jackson Laryngeal, Straight, Ebonized, 2 mm Cup, 200 mm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-01-31 | Aesculap Inc | The forceps have been used in ways not covered by the design resulting in breakage of the clamps. |
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.