Reported Jan 15, 2025 · Ongoing

Tec 850 ISO Anesthesia Vaporizer, Reference Number 1177-9850-ISO

GE Medical Systems, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: GE Medical Systems, LLC · 3000 N Grandview Blvd · Waukesha, WI · 53188-1615

Is this the product you have?

    • Tec 850 ISO Anesthesia Vaporizer
    • Reference Number 1177-9850-ISO
Lot codes and dates
  • GTIN00840682124751
  • Serial Numbers

    1,594 of 1,594 codes

    • SQAC00742
    • SQAC00743
    • SQAC00749
    • SQAC01478
    • SQAC01480
    • SQAC01482
    • SQAC01483
    • SQAC01484
    • SQAC01485
    • SQAC01486
    • SQAC01100
    • SQAD01228
    • SQAC00649
    • SQAD00303
    • SQAD01180
    • SQAD01191
    • SQAD00165
    • SQAD00170
    • SQAC00944
    • SQAD00135
    • SQAD00148
    • SQAD01165
    • SQAC01012
    • SQAC01014
    • SQAD00107
    • SQAD00758
    • SQAD00767
    • SQAD00790
    • SQAC01172
    • SQAC00827
    • SQAC00835
    • SQAD00497
    • SQAC01111
    • SQAC01160
    • SQAC01180
    • SQAC01182
    • SQAC01183
    • SQAC00902
    • SQAC00904
    • SQAD00674
    • SQAD00677
    • SQAC00976
    • SQAD01129
    • SQAD01143
    • SQAD00045
    • SQAD00047
    • SQAD00181
    • SQAD00187
    • SQAC01376
    • SQAC01379
    • SQAC00666
    • SQAC00668
    • SQAC01019
    • SQAD00161
    • SQAD00168
    • SQAD00169
    • SQAD00178
    • SQAD00179
    • SQAC00908
    • SQAC00584
Amount recalled
1594 units

This recall covers 8 products

The agency filed one notice per product. You are reading one of them; the other 7 are below.

Where it was sold

  • Nationwide

Why it was recalled

Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:35 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.