RecallRadar

FDA Device recall Z-0089-2025

Leica Biosystems Cryostat Model Number CM1950, Material Numbers: a) 14047742467, b) 1491950C1US, c) 1491950C2US, d) 1491950C3US

On 2024-10-23 the FDA classified a Class II recall of Leica Biosystems Cryostat Model Number CM1950, Material Numbers: a) 14047742467, b) 1491950C1US, c) 1491950C2US, d) 1491950C3US by Leica Biosystems Nussloch, citing as part of our post market surveillance, we recognized that some customers are using flammable freezing sprays within the cryostat chamber. All flammable freezing sprays can poten….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0089-2025
ClassificationClass II
Statusongoing
Initiated2024-09-04
Published2024-10-23
Last updated2026-09-13 11:57 UTC
CompanyLeica Biosystems Nussloch
DistributionUS

Product

Leica Biosystems Cryostat Model Number CM1950, Material Numbers: a) 14047742467, b) 1491950C1US, c) 1491950C2US, d) 1491950C3US; for freezing and sectioning tissue samples

Reason

As part of our post market surveillance, we recognized that some customers are using flammable freezing sprays within the cryostat chamber. All flammable freezing sprays can potentially ignite and therefore can cause serious injuries. The flammability is indicated on the labelling of these sprays. The cryostat labelling, however, did not include any specific warning about usage of flammable freezing sprays prior to 2019.

Identifiers

code_info
a) Material Number 14047742467, UDI/DI 04049188053992, Serial Numbers: 492102008; b) Material Number 1491950C1US, UDI…a) Material Number 14047742467, UDI/DI 04049188053992, Serial Numbers: 492102008; b) Material Number 1491950C1US, UDI/DI 04049188002501, Serial Numbers: 432082008, 288032008, 581122008, 435082008, 380, 215012008, 427082008, 218012008, 287032008, 216012008, 291042008; c) Material Number 1491950C2US, UDI/DI 04049188002488, Serial Numbers: 524112008, 451082008, 420, 335, 476, 454, 398, 399072008; d) Material Number 1491950C3US, UDI/DI 04049188002464. Serial Numbers: 314042008, 508, 249032008, 318042008, 429, 328052008, 577122008, 407072008, 391072008, 356062008,

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0089-2025%22

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