Howmedica recalls Triathlon Universal Baseplate Size 4 (part 5521-B-400) due to incorrect labeling causing confusion with Size 3 models. Affected units may have wrong lot numbers.
Stryker has identified that 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).
Howmedica is recalling Triathlon Universal Baseplate Size 4 (part number 5521-B-400) because some packaging labels it as Size 3 instead of Size 4. This confusion could lead to using the wrong size plate, which might not fit properly in medical devices.
The baseplate is labeled incorrectly in packaging. Some units labeled as Size 4 actually contain Size 3 parts (lot UZD9IB), and vice versa. This mix-up could cause improper fitting during medical procedures.
Patients using this baseplate for medical procedures may be affected if they receive the wrong size. Surgeons and medical staff who handle these plates are most at risk of using incorrect models.
Check for part number 5521-B-400 on the baseplate. Look for lot number TYX7OB on the packaging. The baseplate may be labeled as Size 3 but contain Size 4 parts.
Verify the baseplate's lot number and part number to confirm it matches the correct specifications.
The recall is due to incorrect labeling where some packaging for Size 4 baseplates contains Size 3 parts and vice versa, potentially causing improper fitting.
Check the lot number and part number on the baseplate and packaging. If it matches the recalled specifications, contact Howmedica for guidance.
The recall addresses labeling confusion, not an immediate safety hazard. Using the wrong size could cause improper fitting but does not pose a direct risk of injury.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-2462-2026 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-2462-2026 from Howmedica. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
