Stradis Medical, LLC dba Stradis Healthcare recalls
Every recall we track for Stradis Medical, LLC dba Stradis Healthcare — 93 in all, from 2021–2022 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Stradis Medical, LLC dba Stradis Healthcare peaked in 2022 (86); 93 since 2017.
All FDA recall records for Stradis Medical, LLC dba Stradis Healthcare 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.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 2 | 5 | 7 |
| 2022 | 0 | 3 | 81 | 2 | 86 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Stradis Medical, LLC dba Stradis Healthcare recalls
What to do if you have a recalled Stradis Medical, LLC dba Stradis Healthcare 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.
All Stradis Medical, LLC dba Stradis Healthcare recalls
5 shown- Lower riskMedical device
Stradis Medical, LLC dba Stradis Healthcare recalls HENRY SCHEIN, Vas Reversal Pack, Item No.888-2549,
Stradis Healthcare recalls Vas Reversal Pack (Item 888-2549) due to potential sterility breaches from incomplete bag sealing. Affected units have specific serial numbers and were sold through Henry Schein.
Stradis HealthcareNov 2, 2022 - UnratedMedical device
Stradis Medical, LLC dba Stradis Healthcare recalls NARMD MEDICAL DEPOT Forceps - Kelly Straight 5.5"; Part Number: ZZ-0700
Stradis Healthcare recalls Kelly Straight 5.5" forceps (part ZZ-0700) due to potential sterile barrier compromise. Affected lots: 22145487092 and 22154486659. No remedy specified in recall notice.
Stradis HealthcareJul 25, 2022 - Lower riskMedical device
Stradis Medical, LLC dba Stradis Healthcare recalls Coryell Memorial Hosp Total, Joint Pack - Surgical Kit
Stradis Healthcare recalls Coryell Memorial Hosp Total, Joint Pack Surgical Kits with possible outer bag perforations that could breach sterility. Affected units include specific lot numbers and SKUs.
Stradis HealthcareFeb 25, 2022 - Lower riskMedical device
Stradis Medical, LLC dba Stradis Healthcare recalls Custom Assemblies, Inc., Single Spike Tumescent Set w/o Chamber, Reorder Number CMS-1212NS Bulk
Stradis Healthcare recalls bulk non-sterile Custom Assemblies Single Spike Tumescent Set (Reorder CMS-1212NS) due to incorrect distribution. This poses infection risk if used for sterile procedures.
Stradis HealthcareOct 28, 2021 - UnratedMedical device
Stradis Medical, LLC dba Stradis Healthcare recalls Foundation Kit
Stradis Healthcare recalls Foundation Kit (Part A10) due to unconfirmed compliance with design and manufacturing standards. Consumers should check product details and follow official instructions.
Stradis HealthcareSep 10, 2021
Stradis Medical, LLC dba Stradis Healthcare recall questions
How many recalls has Stradis Medical, LLC dba Stradis Healthcare had?
93 recalls from Stradis Medical, LLC dba Stradis Healthcare are on record with U.S. safety agencies, from 2021–2022.
What is the most recent Stradis Medical, LLC dba Stradis Healthcare recall?
Stradis Medical, LLC dba Stradis Healthcare recalls HENRY SCHEIN, Vas Reversal Pack, Item No.888-2549,, dated Nov 2, 2022. Every Stradis Medical, LLC dba Stradis Healthcare recall is listed on this page, newest first.
Why are Stradis Medical, LLC dba Stradis Healthcare products recalled?
The most common reasons on record: The sterile barrier may be compromised. (3).
What should I do if I have a recalled Stradis Medical, LLC dba Stradis Healthcare 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 Stradis Medical, LLC dba Stradis Healthcare 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.