---
title: "RSP Humeral Socket Insert Size 36mm Semi-Constrained +4 mm, REF: 509-01-436, ... — FDA record Z-0282-2024 | Is It on Recall"
description: "Two different humeral socket Insert devices were swapped during packaging, which could result in surgeons not having the correct device for surgery, which could"
url: https://isitonrecall.com/recall/fda-device-z-0282-2024-rsp-humeral-socket-insert-size-36mm-semi-constrained-4-mm-ref-509-01-436-orthopedic-shoulder-implant/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# RSP Humeral Socket Insert Size 36mm Semi-Constrained +4 mm, REF: 509-01-436, orthopedic shoulder implant component. — FDA record Z-0282-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Sep 25, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: RSP Humeral Socket Insert Size 36mm Semi-Constrained +4 mm, REF: 509-01-436, orthopedic shoulder implant component.
- **Reason**: Two different humeral socket Insert devices were swapped during packaging, which could result in surgeons not having the correct device for surgery, which could cause a delay in surgery.
- **Classification**: Class II
- **Recalling firm**: Encore Medical, LP
- **Quantity**: 20
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0282-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0282-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI-DI: 00888912144667, Lot: 390P1157 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US: MN, TX, IN, OH, SC, RI, ME, NJ, NY, KS, LA, FL, CA

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [California](https://isitonrecall.com/state/california/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Indiana](https://isitonrecall.com/state/indiana/)
- [Kansas](https://isitonrecall.com/state/kansas/)
- [Louisiana](https://isitonrecall.com/state/louisiana/)
- [Maine](https://isitonrecall.com/state/maine/)
- [Minnesota](https://isitonrecall.com/state/minnesota/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Rhode Island](https://isitonrecall.com/state/rhode-island/)
- [South Carolina](https://isitonrecall.com/state/south-carolina/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Nov 15, 2023
- **Recall initiation date**: Sep 25, 2023
- **Center classification date**: Nov 8, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0282-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Encore Medical, LP records](https://isitonrecall.com/brand/encore-medical-lp/)