---
title: "Atlan, Gas Machine for Anesthesia or Analgesia, Catalog numbers 8621500 (Atla... — FDA record Z-0971-2024 | Is It on Recall"
description: "Internal backup battery may fail spontaneously while the Atlan is being operated without AC mains supply, resulting in unexpected shutdown of the device while r"
url: https://isitonrecall.com/recall/fda-device-z-0971-2024-atlan-gas-machine-for-anesthesia-or-analgesia-catalog-numbers-8621500-atlan-a350-and-8621600-atlan-a/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Atlan, Gas Machine for Anesthesia or Analgesia, Catalog numbers 8621500 (Atlan A350) and 8621600 (Atlan A350 XL) — FDA record Z-0971-2024

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 Nov 17, 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**: Atlan, Gas Machine for Anesthesia or Analgesia, Catalog numbers 8621500 (Atlan A350) and 8621600 (Atlan A350 XL)
- **Reason**: Internal backup battery may fail spontaneously while the Atlan is being operated without AC mains supply, resulting in unexpected shutdown of the device while running on batteries.
- **Classification**: Class II
- **Recalling firm**: Draegerwerk Ag & Co. Kgaa
- **Quantity**: 50 imported to US, not distributed to end users
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0971-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0971-2024%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: 04048675556176 (Atlan A350) 04048675556183 (Atlan A350 XL) Lots: ASSH-0220 ASSH-0221 ASSH-0222 ASSH-0223 ASSH-0224 ASSH-0225 ASSH-0226 ASSH-0227 ASSH-0228 ASSH-0229 ASSH-0230 ASSH-0231 ASSH-0232 ASSH-0233 ASSH-0234 ASSH-0235 ASSH-0236 ASSH-0237 ASSH-0238 ASSH-0239 ASSH-0240 ASSH-0241 ASSH-0242 ASSH-0243 ASSH-0244 ASSH-0245 ASSH-0246 ASSH-0247 ASSH-0248 ASSH-0249 ASSH-0250 ASSH-0251 ASSH-0252 ASSH-0253 ASSH-0254 ASSL-0347 ASSL-0347 ASSL-0349 ASSL-0350 ASSL-0351 ASSL-0352 ASSL-0353 ASSL-0354 ASSL-0355 ASSL-0356 ASSL-0357 ASSL-0358 ASSL-0359 ASSL-0360 ASSL-0361 |

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

## Distribution

No devices were distributed to end-users (customers) in the US. All devices are currently under the direct control of Draeger, Inc.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Feb 7, 2024
- **Recall initiation date**: Nov 17, 2023
- **Center classification date**: Feb 1, 2024

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-0971-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Draegerwerk Ag & Co. Kgaa records](https://isitonrecall.com/brand/draegerwerk-ag-co-kgaa/)