DePuy CORAIL HIGH OFFSET STEM Collarless Size 14 Recall: Incorrect Product in Package
DePuy recalls CORAIL HIGH OFFSET STEM Collarless Size 14 (Part No. L20314, Lot No. 5292130) due to incorrect product being shipped in the package. Consumers should check their order details.
Lower-risk recall
Incorrect device in the package. A package that was labeled as the CORAIL COXA VARA HIGH OFFSET STEM Collared Size 9 (Part No. 3L93709 / Lot No. 5291990), contained the CORAIL HIGH OFFSET STEM Collarless SIZE 14 (Part No. L20314 / Lot No. 5292130).
Contact the company
What happened, in plain English
DePuy is recalling a specific size of CORAIL HIGH OFFSET STEM Collarless implant because the wrong product was shipped in the package. This means customers may have received a size 14 instead of the intended size 9. The recall does not pose a safety risk but requires customers to verify their order details. Read more at govinfonow.com/recall/73436-depuy-corail-high-offset-stem-collarless-size-14-recall-incorrect.
Source Summary by GovInfoNow · govinfonow.com/recall/73436-depuy-corail-high-offset-stem-collarless-size-14-recall-incorrect · Updated September 21, 2026 · FDA enforcement record: FDA #Z-0594-2018
Cite this page
“DePuy CORAIL HIGH OFFSET STEM Collarless Size 14 Recall: Incorrect Product in Package.” GovInfoNow, updated September 21, 2026. https://govinfonow.com/recall/73436-depuy-corail-high-offset-stem-collarless-size-14-recall-incorrect. Based on FDA recall #Z-0594-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0594-2018%22&limit=1).
Why it’s dangerous
The recall involves an incorrect product being shipped in the package. Specifically, a package labeled for CORAIL COXA VARA HIGH OFFSET STEM Collared Size 9 was shipped with CORAIL HIGH OFFSET STEM Collarless Size 14. This mismatch could lead to the wrong implant being used in surgery.
Who’s affected
Customers who purchased the CORAIL HIGH OFFSET STEM Collarless Size 14 (Part No. L20314, Lot No. 5292130) from DePuy Orthopaedics. Patients who received the size 14 implant instead of the size 9 are most at risk of receiving the wrong implant.
How to tell if you have this one
Check your implant's part number (L20314) and lot number (5292130). The product was sold by DePuy Orthopaedics and shipped with the incorrect size (14 instead of 9).
- Brand
DePuy- Category
Medical device
All 2 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
Terminated- Distribution
Nationally; US Consignees for this recall are the affected are US Distributors and US Medical Facilities (Hospitals/User Facilities) that may have purchased, used, or received the affected device.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-0593-2018 | CORAIL COXA VARA HIGH OFFSET STEM Collared Size 9; Part No. 3L93709 and Lot No. 5291990 | 21 Units |
| Z-0594-2018 | CORAIL HIGH OFFSET STEM Collarless SIZE 14; Part No. L20314 and Lot No. 5292130 | 19 |
What to do — step by step
Check Your Implant Details
Verify the part number (L20314) and lot number (5292130) on your implant packaging.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationally; US Consignees for this recall are the affected are US Distributors and US Medical Facilities (Hospitals/User Facilities) that may have purchased, used, or received the affected device.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 22 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Is there a risk of injury from this product?
The recall does not indicate a safety risk. The issue is a mismatch in the product shipped, not a hazard that could cause injury.
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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-0594-2018 (July 12, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0594-2018 to see it in context.
- Plain-language summary written by qwen3:4b on September 21, 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.