---
title: "SteriSpine PS kit of 2 Multi-Axial Fenestrated Screws, model numbers/REF numb... — FDA record Z-1572-2022 | Is It on Recall"
description: "The type of screw printed on the traceability record for the patient label is incorrect, but the type of screw printed on the other labeling is correct."
url: https://isitonrecall.com/recall/fda-device-z-1572-2022-sterispine-ps-kit-of-2-multi-axial-fenestrated-screws-model-numbers-ref-numbers-kitm640-kitm645-and/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# SteriSpine PS kit of 2 Multi-Axial Fenestrated Screws, model numbers/REF numbers KITM640, KITM645, and KITM740. — FDA record Z-1572-2022

Reported completed

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 Jun 3, 2022. 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**: SteriSpine PS kit of 2 Multi-Axial Fenestrated Screws, model numbers/REF numbers KITM640, KITM645, and KITM740.
- **Reason**: The type of screw printed on the traceability record for the patient label is incorrect, but the type of screw printed on the other labeling is correct.
- **Classification**: Class II
- **Recalling firm**: SAFE ORTHOPAEDICS LLC
- **Quantity**: 8 devices
- **Agency-reported status**: Completed
- **Source record identifier**: Z-1572-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1572-2022%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 | KITM640: Lot numbers BF0A07 and 15BF001/R10; UDI 03760219910053; KITM645: Lot number BG0A02; UDI 03760219910060; and KITM740: Lot number BL0A01; UDI 03760219910091. |

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

## Distribution

Distribution was made to MD. There was no government/military distribution.

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

- [Maryland](https://isitonrecall.com/state/maryland/)

## Dates in the source

- **Report date**: Aug 31, 2022
- **Recall initiation date**: Jun 3, 2022
- **Center classification date**: Aug 24, 2022

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-1572-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [SAFE ORTHOPAEDICS LLC records](https://isitonrecall.com/brand/safe-orthopaedics-llc/)