Recall Z-1548-2022— Trinity Sterile, Inc.
Class II · Terminated
Class II FDA medical device recall by Trinity Sterile, Inc., initiated 2022-06-29, terminated 2024-05-10. FDA's recall record names no specific 510(k) clearance for this event. Product: Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number: 96-1708. Reason: 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.
- Recalling firm
- Trinity Sterile, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2022-06-29
- Terminated
- 2024-05-10
- Firm location
- Salisbury, MD, United States
Product description
Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number: 96-1708
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
Data sourced from openFDA. This site is unofficial and independent of the FDA.