Halyard TOTAL JOINT Medical Kit Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
AVID Medical, Inc. is recalling 130 Halyard TOTAL JOINT kits due to labeling that fails to identify natural rubber latex in the StatLock component.
FDA recall: what the record actually shows
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.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
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, medical-devices.
What Happened
AVID Medical, Inc. initiated a voluntary recall of Halyard TOTAL JOINT medical kits because the labeling does not identify that the StatLock component contains natural rubber latex.
Which Products Are Affected
- Product: Halyard TOTAL JOINT
- Model/Catalog Number: MSBM036-03
- Lot Number: 1673233
- UDI: 10809160457887
- Quantity: 130 kits
- Distribution: US Nationwide in the states of MS and TX
- Recall Number: Z-3010-2026
What You Should Do
Consumers should follow instructions provided by the recalling firm regarding the affected kits.
Why This Matters
This Class II recall addresses a labeling deficiency in medical kits distributed in Mississippi and Texas.
Source
FDA recall Z-3010-2026 (https://www.fda.gov/safety/recalls)
Original source: FDA Official Notice ↗
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Elsewhere in the country: similar length or severity timing 8
Two cross-category peer sets, both computed from Areazine's own archive: notices with a similar body length, and notices near the same severity and agency date. These are drawn from other categories, not the same-feed Related list above.
Similar body length
Nearest notices by article body length (766 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to September 9, 2026.
Common Questions
Questions readers often have about this FDA recall.