STARDRIVE SCRWDRVR SHFT/T4 50MM/SELF-RETAINING/HXC-Intended for tightening, loosening, or removing of screw implants during orthopaedic surgery. Part Number: 03.130.010
FDA Recall Z-1916-2024 · Posted 2024-05-28
Recalling FirmSynthes (USA) Products LLC
Recall StatusOpen, Classified
Product CodeHXX
Date Initiated2024-04-25
Product Quantity261 units
Reason for Recall
Stardrive Screwdrivers manufactured without a 5-degree relief cut around the tip and will not engage with their respective 1.3mm and 1.5mm screws, may result in surgical delay
Firm Action
DePuy Synthes issued Urgent Medical Device Recall (Removal) Letter on 4/26/24. Letter states reason for recall, health risk and action to take:
Examine your inventory to determine if you have the subject product lots and quarantine them
immediately. DO NOT USE THE SUBJECT PRODUCTS.
2. Contact your DePuy Synthes Sales Consultant or contact the customer support services at ra-dpyuscsspecial@
its.jnj.com to coordinate the return/credits of the subject product lots.
3. Review, complete, sign, and return the attached Business Response Form (page 3 of this letter) to OneMDField-
[email protected] within three (3) business days of receipt of this notification. Please include in the
email subject: FA 2363331.
4. Please complete the attached Business Response Form even if you do not have the subject product lots on
hand.
5. Forward this notice to anyone in your facility that needs to be informed (e.g., those who manage, transport,
store, stock, or use the subject products).
6. If any of the subject product lots have been forwarded to another facility, contact that facility and provide
them with this notice.
7. Post a copy of this notice in a visible area for awareness and keep a copy for your records.
If you have any questions,
please contact your local DePuy Synthes Sales Consultant. For Medical Information request, please visit our website: https://www.jnjmedicaldevices.com/mir.
Root Cause
Process change control
Distribution Pattern
Worldwide distribution - US Nationwide and the country of Canada.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.