Data Foundry

Medical device recalls 2014

Upgrade Kit — Class II medical device recall Z-0917-2014

Terminated recall by GE Healthcare, reported 2014-02-12, distributed nationwide. Medical device adjustment knob may be loose and affect the accuracy of blended Air/Oxygen gas mixture to patie

Recall numberZ-0917-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmGE Healthcare, Laurel, MD, United States
Recall initiated2013-12-12
Classified2014-02-03
Reported by FDA2014-02-12
Terminated2015-06-01
DistributedNationwide (US)
Countries outside the USAE, AT, AU, BE, BH, BO, CA, CH, CL, CN, CR, CY, CZ, DE, DK, DZ, EE, EG, ES, FI, FR, GB, GR, GT, HK, HN, HU, ID, IE, IL, IN, IQ, IT, KR, KW, LT, MA, MX, MY, NG, NL, NO, NZ, PE, PH, PL, PT, RO, RU, SA, SE, SG, SK, TH, TN, TR, UY, VE, ZA
Quantity561 units
Serial numbers100341, 100342, 100348, 200118, 200143, 200513, 200522, 200590, 200598, 200617, 201111, 201375, 201384, 201409, 201424, 201567, 201621, 201622, 201625, 201627, 201814, 202013, 202021, 202141, 202143 and 475 more
Model numbersM1139417, M1192226, M1223628

Product

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.

Reason for recall

Medical device adjustment knob may be loose and affect the accuracy of blended Air/Oxygen gas mixture to patients.

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-0917-2014. 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.