Home › ASPEN SURGICAL PRODUCTS, INC. › Symmetry Blumenthal
Symmetry Blumenthal
ASPEN SURGICAL PRODUCTS, INC. · Model 30-2547 · UDI-DI 00887482145814
HTX
Prescription
5
510(k) clearances
618
Adverse events (2 deaths)
7
Recalls
329
Facilities
Description
Symmetry® Rongeur, Blumenthal Bone, 30° Angle, 4 mm Jaw, 6 1/4 in
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
| 2017-05-25 | Exactech, Inc. | Instructions for use (IFU) is updated to clarify the proper technique and instrumentation to ream the Glenoid, i.e., to include a caution statement that the surgeon should ream on- |
| 2017-05-25 | Exactech, Inc. | Instructions for use (IFU) is updated to clarify the proper technique and instrumentation to ream the Glenoid, i.e., to include a caution statement that the surgeon should ream on- |
| 2017-05-25 | Exactech, Inc. | Instructions for use (IFU) is updated to clarify the proper technique and instrumentation to ream the Glenoid, i.e., to include a caution statement that the surgeon should ream on- |
| 2017-05-25 | Exactech, Inc. | Instructions for use (IFU) is updated to clarify the proper technique and instrumentation to ream the Glenoid, i.e., to include a caution statement that the surgeon should ream on- |
| 2017-05-25 | Exactech, Inc. | Instructions for use (IFU) is updated to clarify the proper technique and instrumentation to ream the Glenoid, i.e., to include a caution statement that the surgeon should ream on- |
| 2017-05-25 | Exactech, Inc. | Instructions for use (IFU) is updated to clarify the proper technique and instrumentation to ream the Glenoid, i.e., to include a caution statement that the surgeon should ream on- |
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.