Halyard TOTAL JOINT Kit Recall for Labeling Deficiency
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AVID Medical, Inc. is recalling 63 Halyard TOTAL JOINT kits (Model MSBM036-03, Lot 1632948) distributed in MS and TX due to missing latex warning on labeling.
The full picture behind this FDA recall
This notice was issued by FDA on September 9, 2026 and geographically references Mississippi, Texas. The FDA classifies this as a Class II recall, with the stated reason "Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.", distributed us nationwide distribution in the states of ms, tx.. FDA recall classes run from I (reasonable probability of serious harm) to III (unlikely to cause harm), so the class number is the fastest way to gauge severity here. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
It is tempting to skim, check personal relevance, and move on. The better habit is confirming scope, source, and timestamp first, then reading this alongside related notices instead of drawing a conclusion from one record alone.
The original agency source is linked below so you can verify this record directly before acting on it. Its related labels are recall, product-safety, fda, Devices.
What Happened
The recall was initiated due to a labeling deficiency: the medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Which Products Are Affected
Halyard TOTAL JOINT, Model/Catalog Number: MSBM036-03. Lot Code: Lot Number 1632948, UDI 10809160423578. A total of 63 kits are affected. Distribution was to US Nationwide in the states of MS and TX.
What You Should Do
Consumers should verify the lot number on affected kits and contact AVID Medical, Inc. for return or refund instructions.
Why This Matters
The labeling omission may pose a risk to individuals with latex allergies using the medical kits.
Source
FDA recall number Z-3006-2026
Original source: FDA Official Notice ↗
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Similar notices nationwide by length or severity timing 8
Beyond this FDA recall's own category, Areazine surfaces two nationwide peer sets: length-matched and severity/date-matched notices from elsewhere in the archive, distinct from the same-feed Related list above.
Similar body length
Nearest notices by article body length (710 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to September 9, 2026.
Questions & Answers
Common questions about this FDA recall.