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POWER DRIVE ART1
Richard Wolf GmbH · Model 2304007 · UDI-DI 04055207012246
10
510(k) clearances
18,245
Adverse events
27
Recalls
147
Facilities
Description
MOTOR CONTROL UNIT 2304 for Orthopedics, Spine surgery and Bronchoscopy, for connection of handpieces M4, M5/0, M5/3, S1 and M1, connection for two handpieces and a footswitch, 5.7 inch monochrome Display, compatible with core, U: 120VAC, 50/60Hz, Dim. (wxhxd): 330x155x365mm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-02-15 | Pro-Dex Inc | Battery packs used in surgical procedures where a surgeon uses a powered screwdriver and a right-angle attachment have switched manufacturing and expiration dates on sterile pouch |
| 2018-09-25 | Pro-Dex Inc | Visual particulates within a battery Tyvek pouch. The battery is provided sterile for use with surgical drivers. |
| 2017-03-28 | Aesculap Implant Systems LLC | Diamond particulates may break off the burr and fall into the surgical site. If the particles are not detected and are not removed from the surgical site a foreign body reaction m |
| 2017-03-28 | Aesculap Implant Systems LLC | Diamond particulates may break off the burr and fall into the surgical site. If the particles are not detected and are not removed from the surgical site a foreign body reaction m |
| 2017-03-28 | Aesculap Implant Systems LLC | Diamond particulates may break off the burr and fall into the surgical site. If the particles are not detected and are not removed from the surgical site a foreign body reaction m |
| 2016-10-06 | The Anspach Effort, Inc. | Supplied Directions for Use (DFU) did not contain a recommended service interval. |
| 2016-10-06 | The Anspach Effort, Inc. | Supplied Directions for Use (DFU) did not contain a recommended service interval. |
| 2016-10-06 | The Anspach Effort, Inc. | Supplied Directions for Use (DFU) did not contain a recommended service interval. |
| 2016-10-06 | The Anspach Effort, Inc. | Supplied Directions for Use (DFU) did not contain a recommended service interval. |
| 2016-10-06 | The Anspach Effort, Inc. | Supplied Directions for Use (DFU) did not contain a recommended service interval. |
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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.