Reported Feb 12, 2014 · Terminated
Upgrade Kit, Resuscitation, T-Piece, part numbers M1139417, M1192226 and M1223628, labeled in part ***GE Healthcare…
GE Healthcare
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 Healthcare · 8880 Gorman Rd · Laurel, MD · 20723-5800
Is this the product you have?
- Upgrade Kit, Resuscitation, T-Piece, part numbers M1139417, M1192226 and M1223628, labeled in part ***GE Healthcare 8880 Gorman Road Laurel, MD 20723 ***www.gehealthcare.com*** Provides the basic equipment required for pulmonary resuscitation of infants.
- Lot codes and dates
- Serial Numbers
561 of 561 codes
100341100342100348200118200143200513200522200590200598200617201111201375201384201409201424201567201621201622201625201627201814202013202021202141202143202147202280202300202365202395202439202538203117203186203419203448203452203453203755203961204048204153204154204166204170204323204333204732204848204858204882204888204896204898204904204906204908205060205062205074
- Serial Numbers
- Amount recalled
- 561 units
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
- Nationwide
- PR
Why it was recalled
Medical device adjustment knob may be loose and affect the accuracy of blended Air/Oxygen gas mixture to patients.
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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