---
title: "OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product, Product code MG412143 — FDA record Z-1057-2022 | Is It on Recall"
description: "Disconnection of the OnGuard2 Bag Adaptor SP from infusion bags which may result in spillage of hazardous medications."
url: https://isitonrecall.com/recall/fda-device-z-1057-2022-onguard2-cstd-bag-adaptor-sp-a-chemfort-cstd-product-product-code-mg412143/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product, Product code MG412143 — FDA record Z-1057-2022

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 Mar 8, 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**: OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product, Product code MG412143
- **Reason**: Disconnection of the OnGuard2 Bag Adaptor SP from infusion bags which may result in spillage of hazardous medications.
- **Classification**: Class II
- **Recalling firm**: SIMPLIVIA HEALTHCARE LTD.
- **Quantity**: 293,520
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1057-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1057-2022%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 | UDI: 37290115921435, Lots: UBE507, UBE508, UBE513, UBE516, UBE517, UBE509, UBE511, UBE512, UBE514, UBE515, UBE517, UBE518, UBE526, UBE530, UBE531, UBE534, UBE533, UBE535, UBE536 |

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

## Distribution

Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY.

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

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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: May 18, 2022
- **Recall initiation date**: Mar 8, 2022
- **Center classification date**: May 11, 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-1057-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [SIMPLIVIA HEALTHCARE LTD. records](https://isitonrecall.com/brand/simplivia-healthcare-ltd/)
