Class II U.S. Food and Drug Administration

Onkos Surgical Inc. My3D recall: Personalized pelvic implants inadvertently mixed up and distributed

Recall published 11 days ago

Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers.

The hazard: Device safety concern

A device recall was filed for this product. For anything implanted or relied on daily, the clinician comes before the paperwork.

What the notice says: Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers.

Why it matters: The FDA recorded an enforcement action against this device. Most device recalls are corrections rather than removals, so the device often stays in use while the manufacturer issues a fix.

Recall details

Recall number
Z-0090-2027
Published
October 14, 2026
Risk level
Class II
Status
Ongoing
Issued by
U.S. Food and Drug Administration
Brand
Onkos Surgical, Inc.
Product type
Medical devices
Units affected
1 implant
Distribution
Nationwide
Made in
United States
Lot / code info
UDI: B278PVACREC04M0-Lot# C26-0346; Case# C26-0346,

Products covered by this recall

Onkos Surgical Inc. My3D Personalized Pelvic Implant, Porous, Left REF PV-ACREC-04M

Check your product

The notice names 2 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.

Lot or batch code

Usually ink-stamped near the seam, the cap or the bottom of the pack.

  • C26-0346

Model or item number

On the rating label, the box or the instruction sheet.

  • PV-ACREC-04M — UDI

Codes are lifted verbatim from the FDA — Device enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.

What to do about Device

Onkos Surgical, Inc. — A device recall was filed for this product. For anything implanted or relied on daily, the clinician comes before the paperwork.

  1. Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.
  2. Ask the supplier or clinic that provided it what the remedy is in your case.
  3. If you are a facility, quarantine affected stock and log the correction.
  4. Report device problems to the FDA through MedWatch.

Claiming on a recalled device

Device recalls are tracked by serial and lot number, so your claim moves faster if you lead with those.

  • Have the model, catalogue, lot and serial numbers ready before you call — they are on the device label or its box.
  • Ask explicitly whether your unit is in the affected range; many recalls cover only part of a model line.
  • If you need the device daily, ask what interim arrangement they offer while the remedy is carried out.
  • Log the date, the name and the reference number of every call. Device recalls can run for months.

Company contact: Onkos Surgical, Inc. — 77 E Halsey Rd, Parsippany, NJ, 07054-3714

The official notice

This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.

Open the FDA — Device enforcement record U.S. Food and Drug Administration recalls

Questions people ask about this recall

Why was Onkos Surgical, Inc. medical devices recalled?

Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers. Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers.

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: lot code C26-0346; model number PV-ACREC-04M — UDI. If the code on your package is not on that list, your unit is outside the recall.

What should I do with it right now?

Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.

Can I get my money back?

Have the model, catalogue, lot and serial numbers ready before you call — they are on the device label or its box.

Where was the recalled product sold?

It was distributed nationwide.

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