AVID Medical Halyard TOTAL JOINT Recall: Latex in Statlock Component
AVID Medical recalls Halyard TOTAL JOINT Model MSBM036-03 due to latex in statlock component. Affected units may cause allergic reactions. Contact for remedy.
Lower-risk recall
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
What happened, in plain English
AVID Medical is recalling Haly: TOTAL JOINT model MSBM036-03 because the statlock component contains natural rubber latex. This could cause allergic reactions in sensitive individuals. The recall affects specific units sold with lot code 1673233. Read more at govinfonow.com/recall/697921-avid-medical-halyard-total-joint-recall-latex-in-statlock-component.
Source Summary by GovInfoNow · govinfonow.com/recall/697921-avid-medical-halyard-total-joint-recall-latex-in-statlock-component · Updated September 14, 2026 · FDA enforcement record: FDA #Z-3010-2026
Cite this page
“AVID Medical Halyard TOTAL JOINT Recall: Latex in Statlock Component.” GovInfoNow, updated September 14, 2026. https://govinfonow.com/recall/697921-avid-medical-halyard-total-joint-recall-latex-in-statlock-component. Based on FDA recall #Z-3010-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3010-2026%22&limit=1).
Why it’s dangerous
The statlock component in the medical kit contains natural rubber latex. People with latex allergies could have reactions like rashes or breathing difficulties when exposed to the latex.
Who’s affected
Patients using the Halyard TOTAL JOINT model MSBM036-03 with lot code 1673233 are at risk of allergic reactions if they have latex sensitivity. Healthcare providers using this device may also be affected.
How to tell if you have this one
Check for the model number MSBM036-03 and lot code 1673233 on the product. The recall applies to specific units sold with this lot code.
- Brand
AVID Medical- Category
Medical device
All 7 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
Ongoing- Distribution
US Nationwide distribution in the states of MS, TX.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-3005-2026 | Brand Name: Halyard Product Name: DAVINCI TRUCUSTOM BUNDLE containing TRAY FOLEY 16FR W/STATLOCK Model/Catalog Number: SAMM064-27; Lot Code: Lot Number: 1634391 UDI: 10809160439708 | 45 kits |
| Z-3006-2026 | Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03; Lot Code: Lot Number: 1632948 UDI: 10809160423578 | 63 kits |
| Z-3007-2026 | Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03; Lot Code: Lot Number: 1649979 UDI: 10809160457887 | 78 kits |
| Z-3008-2026 | Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03; Lot Code: Lot Number: 1654575 UDI: 10809160457887 | 78 kits |
| Z-3009-2026 | Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03; Lot Code: Lot Number: 1662335 UDI: 10809160457887 | 120 Kits |
| Z-3010-2026 | Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03; Lot Code: Lot Number: 1673233 UDI: 10809160457887 | 130 KITS |
| Z-3011-2026 | Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03; Lot Code: Lot Number: 1649519 UDI: 10809160457887 | 78 kits |
What to do — step by step
Check Product Label
Look for the model number MSBM036-03 and lot code 1673233 on the device.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 2 states.
FDA distribution: “US Nationwide distribution in the states of MS, TX.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Mississippi, Texas.
Recall timeline
FDA published this recall 55 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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-3010-2026 (July 9, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3010-2026 to see it in context.
- Plain-language summary written by qwen3:4b on September 14, 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.