Data Foundry

Medical device recalls 2024

Atlan — Class II medical device recall Z-0971-2024

Ongoing recall by Draegerwerk Ag & Co. Kgaa, reported 2024-02-07. Internal backup battery may fail spontaneously while the Atlan is being operated without AC mains supply, resu

Recall numberZ-0971-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmDraegerwerk Ag & Co. Kgaa, Lubeck, Germany
Recall initiated2023-11-17
Classified2024-02-01
Reported by FDA2024-02-07
Quantity50 imported
Reason classesdevice malfunction
UPC / GTIN / UDI-DI04048675556176, 04048675556183
Lot numbersASSH-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-0349, ASSL-0350, ASSL-0351, ASSL-0352 and 9 more
Model numbers8621500

Product

Atlan, Gas Machine for Anesthesia or Analgesia, Catalog numbers 8621500 (Atlan A350) and 8621600 (Atlan A350 XL)

Reason for recall

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0971-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.