Reported Jan 15, 2025 · Ongoing

Tec 820 ISO Anesthesia Vaporizer, Reference Number 1177-9820-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 820 ISO Anesthesia Vaporizer
    • Reference Number 1177-9820-ISO
Lot codes and dates
  • GTIN00840682124744
  • Serial Numbers

    644 of 644 codes

    • SQAD01037
    • SQAD01038
    • SQAD01041
    • SQAC01464
    • SQAC01467
    • SQAC00988
    • SQAC00987
    • SQAD01184
    • SQAD01219
    • SQAD01221
    • SQAD01222
    • SQAC01106
    • SQAD00048
    • SQAD00057
    • SQAD00059
    • SQAD00116
    • SQAD00124
    • SQAD00127
    • SQAD00129
    • SQAD00134
    • SQAD00136
    • SQAD00137
    • SQAD00139
    • SQAD00144
    • SQAD00576
    • SQAD00577
    • SQAD00581
    • SQAC00844
    • SQAC00851
    • SQAC00852
    • SQAC00854
    • SQAC00855
    • SQAC00856
    • SQAC00857
    • SQAC00858
    • SQAC00930
    • SQAC00842
    • SQAC00895
    • SQAC00517
    • SQAC01192
    • SQAD00860
    • SQAC01203
    • SQAC00989
    • SQAC00990
    • SQAC01186
    • SQAD00142
    • SQAD00486
    • SQAD00498
    • SQAD00831
    • SQAD00853
    • SQAD00855
    • SQAD00856
    • SQAD00857
    • SQAD00862
    • SQAD00863
    • SQAD00871
    • SQAD00873
    • SQAD00881
    • SQAD00883
    • SQAD00887
Amount recalled
644 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, 6:56 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.