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Trinity Sterile, Inc. recalls

Every recall we track for Trinity Sterile, Inc. — 10 in all, from 2021–2024 — plus the complaints and injury reports the public filed about them.

10recalls

Recalls per year, by danger level

Recalls from Trinity Sterile, Inc. dropped to zero in 2025 (0, down from 5 in 2024).

2017: 0 recalls20172018: 0 recalls20182019: 0 recalls20192020: 0 recalls20202021: 1 recall — 1 lower risk120212022: 4 recalls — 4 lower risk420222023: 0 recalls20232024: 5 recalls — 5 lower risk520242025: 0 recalls20252026 (to date): 0 recalls2026to date

All FDA recall records for Trinity Sterile, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.

Recalls per year for Trinity Sterile, Inc., by danger level
YearStop using nowUse cautionLower riskNot yet ratedTotal
201700000
201800000
201900000
202000000
202100101
202200404
202300000
202400505
202500000
2026 (to date)00000

Most common reasons for Trinity Sterile, Inc. recalls

  • Potential for hole in package compromising sterility of the medical kit.5

What to do if you have a recalled Trinity Sterile, Inc. product

  1. Match the model, catalog or lot number on your device to the recall.
  2. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
  3. Report problems to FDA MedWatch.

See this week’s new recalls.

All Trinity Sterile, Inc. recalls

3 shown

Trinity Sterile, Inc. recall questions

How many recalls has Trinity Sterile, Inc. had?

10 recalls from Trinity Sterile, Inc. are on record with U.S. safety agencies, from 2021–2024.

What is the most recent Trinity Sterile, Inc. recall?

Trinity Sterile, Inc. recalls Brand Name: Wolf-Pak Product Name: Premium Dressing Change Kit with GuardiVa & Statlock CS/30 Model/Catalog Number:, dated Dec 13, 2024. Every Trinity Sterile, Inc. recall is listed on this page, newest first.

Why are Trinity Sterile, Inc. products recalled?

The most common reasons on record: Potential for hole in package compromising sterility of the medical kit. (5).

What should I do if I have a recalled Trinity Sterile, Inc. product?

Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.

How do I get alerts for new Trinity Sterile, Inc. recalls?

Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.