Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number: 96-1708
This recall has been terminated (originally issued June 29, 2022).
- Company
- Trinity Sterile, Inc.
- Recall Initiated
- June 29, 2022
- Terminated
- May 10, 2024
- Recall Number
- Z-1548-2022
- Quantity
- 5 cases (125 eaches )
- Firm Location
- Salisbury, MD
- Official Source
- View on FDA website ↗
Reason for Recall
Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy
Distribution
US Nationwide distribution in the states of FL, PA.
Lot / Code Info
UDI-DI Number: 50649111317590 Case 10649111317590 Kit Lot Numbers: 600001 600002
Root Cause
Labeling design
Action Taken
Trinity Medical issued Urgent Medical Device Correction Letter dated June 30, 2022 via email as a follow-up to the call on 6/29/22. Letter states reason for recall, health risk and action to take: 1. Inspect your inventory for the affected products and lot numbers identified on the attached spreadsheet. If you have affected stock in inventory, immediately discontinue use and quarantine the products. If you have transferred any of the affected kits to a third party, please communicate this information to them. 2. Notify Trinity. Please complete the enclosed Customer Response Form as soon as possible, indicating whether you understand this medical device correction. Fax it to 410-860-2913 or email it to customerservice@trinitysterile.com. 3. Relabel the affected product. Once Trinity receives your completed Customer Response Form, Trinity will provide you with brightly colored stickers to attach to each case and kit. If you have any questions, please contact Customer Service at 410-860-5123.