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CASPAR RETRACTOR FRAME
SONTEC INSTRUMENTS, INC. · Model 416-655 · UDI-DI 00192896037632
FFO
Prescription
5
510(k) clearances
87
Adverse events
3
Recalls
152
Facilities
Description
CASPAR RETRACTOR FRAME DOUBLE ARTICULATION TRANS-VERSE/STEPDOWN CERVICAL VERTEBRAL COLUMN QUICK RELEASE
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
| 2015-11-25 | Abeon Medical Corporation | The firm was notified by some of their customers that some of the sealed pouches contain tears compromising the sterility of the product. |
| 2015-11-25 | Abeon Medical Corporation | The firm was notified by some of their customers that some of the sealed pouches contain tears compromising the sterility of the product. |
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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.