Depuy ATTUNE Revision Hinge Femoral LT SZ 8 CEM: Sterility Packaging Risk
Depuy recalls ATTUNE Revision Hinge Femoral LT SZ 8 CEM (Part 150450108) due to potential sterility compromise from packaging adhesion. Affected units have specific lot numbers and expiration dates.
Lower-risk recall
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Contact the company
What happened, in plain English
Depuy is recalling a specific hip implant part because its sterile packaging might stick together, risking infection during surgery. This affects patients who received this exact model with the listed part number. Read more at govinfonow.com/recall/49542-depuy-attune-revision-hinge-femoral-lt-sz-8-cem-sterility.
Source Summary by GovInfoNow · govinfonow.com/recall/49542-depuy-attune-revision-hinge-femoral-lt-sz-8-cem-sterility · Updated August 17, 2026 · FDA enforcement record: FDA #Z-1988-2026
Cite this page
“Depuy ATTUNE Revision Hinge Femoral LT SZ 8 CEM: Sterility Packaging Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/49542-depuy-attune-revision-hinge-femoral-lt-sz-8-cem-sterility. Based on FDA recall #Z-1988-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1988-2026%22&limit=1).
Why it’s dangerous
The external sterile packaging can stick to the internal sterile packaging, which might compromise the sterility of the implant during surgery. This could lead to infection if the implant is not properly sterile.
Who’s affected
Patients who received this specific hip implant part during surgery are affected. Surgeons and hospitals using this part for procedures are most at risk.
How to tell if you have this one
Check for the part number 150450108 on the packaging. Affected units have lot number AF1006441 and expire by December 31, 2035.
- Brand
Depuy- Category
Medical device
All 9 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 MN, NC, TX.
| Recall number | Product, codes & lots |
|---|---|
| Z-1985-2026 | Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 4 CEM. Part Number: 150450104.; Part Number: 150450104. UDI-DI: 10603295533115. Lot Number: 1007844. Expiration Date: 11/30/2035 |
| Z-1986-2026 | Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 5 CEM. Part Number: 150450105.; Part Number: 150450105. UDI-DI: 10603295533122. Lot Number: AF1007829. Expiration Date: 12/31/2035. |
| Z-1987-2026 | Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 7 CEM. Part Number: 150450107.; Part Number: 150450107. UDI-DI: 10603295533139. Lot Number: 1006440. Expiration Date: 11/30/2035. |
| Z-1988-2026 | Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 8 CEM. Part Number: 150450108.; Part Number: 150450108. UDI-DI: 10603295543022. Lot Number: AF1006441. Expiration Date: 12/31/2035. |
| Z-1989-2026 | Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 3 CEM. Part Number: 150450203.; Part Number: 150450203. UDI-DI: 10603295533146. Lot Number: 1007537. Expiration Date: 10/31/2035. |
| Z-1990-2026 | Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 4 CEM. Part Number: 150450204.; Part Number: 150450204. UDI-DI: 10603295533153. Lot Number: 1005229. Expiration Date: 10/31/2035. |
| Z-1991-2026 | Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 5 CEM. Part Number: 150450205.; Part Number: 150450205. UDI-DI: 10603295533160. Lot Number: 1006444. Expiration Date: 10/31/2035. |
| Z-1992-2026 | Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 7 CEM. Part Number: 150450207.; Part Number: 150450207. UDI-DI: 10603295533177. Lot Number: 1007046. Expiration Date: 10/31/2035. |
| Z-1993-2026 | Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 8 CEM. Part Number: 150450208.; Part Number: 150450208. UDI-DI: 10603295543039. Lot Numbers: AF1008441, AF1008028. Expiration Date: 12/31/2035. |
What to do — step by step
Check Packaging Details
Look for part number 150450108, lot number AF1006441, and expiration date December 31, 2035 on the packaging.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 3 states.
FDA distribution: “US Nationwide distribution in the states of MN, NC, TX.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Minnesota, North Carolina, Texas.
Recall timeline
FDA published this recall 33 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Questions people ask
Do I need to stop using this part?
No action is required for the part itself; the recall is for identification and potential replacement if needed.
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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-1988-2026 (April 3, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1988-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 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.