Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number: 96-1708 — FDA record Z-1548-2022

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jun 29, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

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
Classification
Class II
Recalling firm
Trinity Sterile, Inc.
Quantity
5 cases (125 eaches )
Agency-reported status
Terminated
Source record identifier
Z-1548-2022

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityUDI-DI Number: 50649111317590 Case 10649111317590 Kit Lot Numbers: 600001 600002

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

US Nationwide distribution in the states of FL, PA.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Aug 24, 2022
Recall initiation date
Jun 29, 2022
Center classification date
Aug 18, 2022
Termination date
May 10, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

Related records