Clear View Black Belt Retractor Basic Set
KOROS U.S.A., INC. · Model 7320-00T · UDI-DI 10840199501790
Description
Clear View Black Belt Retractor Basic Set, Consists of the Following: 1x 7320-22T - Korpectomy Retractor frame Right, 1x 7320-20T - Retractor frame Left, 1x 7320-30T - Retractor frame Offset, 2x 7320-40T - Blade Inserting Clamp, 2x 7322-34T - Pronged Ti Blade 34mm, 2x 7322-40T - Pronged Ti Blade 40mm, 2x 7322-45T - Pronged Ti Blade 45mm, 2x 7322-50T - Pronged Ti Blade 50mm, 2x 7322-55T - Pronged Ti Blade 55mm, 2x 7322-60T - Pronged Ti Blade 60mm, 2x 7322-70T - Pronged Ti Blade 70mm, 2x 7324-34T - Blunt Ti Blade 34mm, 2x 7324-40T - Blunt Ti Blade 40mm, 2x 7324-45T - Blunt Ti Blade 45mm, 2x 7324-50T - Blunt Ti Blade 50mm, 2x 7324-55T - Blunt Ti Blade 55mm, 2x 7324-60T - Blunt Ti Blade 60mm, 2x 7324-70T - Blunt Ti Blade 70mm, 4x 7326-40T - Two-Level Ti Blade Pronged 40mm, 4x 7326-47T - Two-Level Ti Blade Pronged 47mm, 4x 7326-55T - Two-Level Ti Blade Pronged 55mm, 2x 7328-40T - Two-Level Ti Blade Blunt 40mm, 2x 7328-47T - Two-Level Ti Blade Blunt 47mm, 2x 7328-55T - Two-Level Ti Blade Blunt 55mm, 1x 7320-90T - Sterilizing Instrument Case with silicone pads
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. |
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 docs