Trinity Sterile recalls Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number 96-1708 due to natural rubber latex in packaging. Those with latex allergies may face risks. Contact for remedy.
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
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Contact the company
📍Recalling firmTrinity Sterile, Inc.201 Kiley Dr · Salisbury, MD 21801-2249
✎ GovInfoNow plain-language explainer
Trinity Sterile is recalling Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number 96-1708 because the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. This poses a risk to people with latex allergies. The recall is for specific lot numbers and re-order numbers. Read more at govinfonow.com/recall/60405-sklar-instruments-iv-cath-dressing-tray-cs-25-recall-latex.
“Sklar Instruments IV Cath Dressing Tray Cs/25 Recall: Latex Allergy Risk.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/60405-sklar-instruments-iv-cath-dressing-tray-cs-25-recall-latex. Based on FDA recall #Z-1548-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1548-2022%22&limit=1).
The FDA announced on June 29, 2022, that Trinity Sterile, Inc. recalled Sklar Instruments IV Cath Dressing Trays because packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex despite being labeled latex-free. The agency classified the recall as Class II.
How to tell if you have it
Brand: Trinity Sterile
Product: Sklar Instruments IV Cath Dressing Tray Cs/25
The kits are mislabeled as latex-free, but the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. This presents a potential risk to individuals with latex allergies.
Context
GovInfoNow's records show Trinity Sterile, Inc. has two other recalls on record since February 23, 2021. On December 13, 2024, Wolf-Pak issued a recall for Premium Dressing Change Kits due to sterility risks from package holes. On February 23, 2021, Trinity Sterile recalled Midline Catheter Dressing Kits because improper sealing posed an infection risk. Other recent recalls of similar products include Stryker NICO Myriad Handpieces (October 31, 2025), Stryker NICO BrainPath Shephard's Hook (October 31, 2025), and Covidien EndoStitch Polysorb Loading Unit (April 15, 2026).
How to tell if you have this one
Check for the re-order number 96-1708 and lot numbers 600001 or 600002 on the Sklar Instruments IV Cath Dressing Tray Cs/25 packaging.
Brand
Trinity Sterile
Category
Medical device
FDA recall event · 4 products
All 4 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Terminated
Distribution
US Nationwide distribution in the states of FL, PA.
Recall number
Product, codes & lots
Quantity
Z-1548-2022
Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number: 96-1708; UDI-DI Number: 50649111317590 Case 10649111317590 Kit Lot Numbers: 600001 600002
5 cases (125 eaches )
Z-1549-2022
Wolf-Pak Premium Dressing Kit with GuardVA Cs/30 Ref: DC5030LF; UDI-DI: 10850007185760 Case 00850007185763 Kit Lot Numbers: 600000 600001 600002 600003 600004 600005 600006 600007 600008
1,513 cases (45,390 eaches)
Z-1550-2022
Wolf Pak Premium Dressing Change Kit with Statlock CS/30 Ref: DC5040LF; UDI-DI: 10850007185746 Case 00850007185749 Kit Lot Numbers: 600000 600001 600002 600003 600004 600005 600008 600009 600010 600011 600012
2,512 cases (75,360 eaches )
Z-1551-2022
Wolf Pak Premium Dressing Change Kit with GuardVA and Statlok Cs/30 Ref: DC5090LF; UDI-DI: 10850007185722 Case 00850007185725 Kit Lot Numbers: 600000 600001 600002 600003 600004 600005 600008 600009 600010 600011 600012 600013 600014 600015 600017 600018 600019
4,169 cases (125,070 eaches)
Based on the official FDA remedy
What to do — step by step
Check Packaging
Look for the re-order number 96-1708 and lot numbers 600001 or 600002 on the product packaging.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 2 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide distribution in the states of FL, PA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Florida, Pennsylvania.
Recall timeline
FDA terminated this recall 22 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-1548-2022 (June 29, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1548-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.