Triathlon Universal Baseplate Size 4 Recall Issued
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Howmedica Osteonics Corp. is recalling 7 units of TRI TS BASEPLATE SIZE 4 due to incorrect packaging labels mixing Size 3 and Size 4 baseplates.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 3, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. 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.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
Howmedica Osteonics Corp. has initiated a recall because Triathlon Universal Baseplate Size 3 (lot UZD9IB) is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon Universal Baseplate Size 4 (lot TYX7OB) is contained in packaging labeled as Triathlon Universal Baseplate Size 3 (lot UZD9IB).
Which Products Are Affected
The recall involves TRI TS BASEPLATE SIZE 4, Part Number: 5521-B-400, UDI: (01)07613327026061(17)260921(10) TYX7OB, Lot Number: TYX7OB. A total of 7 units were distributed nationwide in the states of AZ, CA, GA, MI, NC, NJ, NY, and WV. The recall number is Z-2462-2026.
What You Should Do
No specific consumer action steps or contact information for returns or refunds are provided in the recall notice.
Why This Matters
The mislabeling may result in the wrong size baseplate being used during procedures.
Source
FDA recall number Z-2462-2026, Class II device recall.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (965 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 3, 2026.
Frequently Asked Questions
Common questions about this FDA recall.