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All Titanium Super Slide III Self Retaining Retractor, Extended Set
KOROS U.S.A., INC. · Model 7329-05M · UDI-DI 10840199500656
GZT
Prescription
1
510(k) clearances
111
Adverse events
6
Recalls
80
Facilities
Description
All Titanium Super-Slide III Retractor Extended Set Consists of the Following: 1x 7329-10m, 4x 7329-82m, 4x 7329-84m, 4x 7329-86m and 4x 7329-87m 2x 7329-60m 2x 7329-62m 2x 7329-68m 1x 7329-90m
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-06-19 | Nico Corp. | Mislabeled hook pouch included a transport/storage label rather than the product label containing key product information such as part number, lot number, and expiration date, etc |
| 2012-08-21 | Vycor Medical, Inc. | Vycor Medical recalled their VBAS (Vycor Viewsite Brain Access System) because an unidentified black fiber was found on the device. |
| 2012-07-17 | Nico Corp. | BrainPath sheaths were mislabeled. Sheaths which measure 50mm were labeled as 60mm. The length callout on the label does not match the actual length of the sheath within the packag |
| 2012-07-17 | Nico Corp. | BrainPath sheaths were mislabeled. Sheaths which measure 50mm were labeled as 60mm. The length callout on the label does not match the actual length of the sheath within the packag |
| 2007-12-19 | Abbott Spine | Dislodged Collar Spring; The collar spring binding on the shaft of generic handle used with multiple surgical instruments has the potential to release the device's internal bearing |
| 2003-02-26 | Ohio Medical Instrument Co Inc | The component was manufactured with an insufficient weld that could break during use. |
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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.