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.