Z-2142-2008

GE Precision MPi, model 5126893. GE Medical Systems - Americas, Milwaukee, USA The product is used to...

Name: Z-2142-2008 GE Precision MPi, model 5126893. GE Medical Systems - Americas, Milwaukee, USA The product is used to...
Creator: GE Healthcare
Published: 2008-05-01
License: https://open.fda.gov/license/

GE Healthcare / initiated 2008-05-01 / Terminated / root cause: labeling and UDI

FDA source

GE Healthcare began a recall of GE Precision MPi, model 5126893. GE Medical Systems - Americas, Milwaukee, USA The product is used to generate radiographic and fluoroscopic images of human... on 2008-05-01. The reason FDA records is "The Precision MPi collimator did not contain a label identifying the device as being certified to comply with applicable requirements of the x-ray performance standard". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as labeling and UDI.

Recall record

Recall number: Z-2142-2008
Status: Terminated
Initiated: 2008-05-01
Posted: 2008-09-19
Terminated: 2011-12-17
Recalling firm: GE Healthcare
Product: GE Precision MPi, model 5126893. GE Medical Systems - Americas, Milwaukee, USA The product is used to generate radiographic and fluoroscopic images of human anatomy, perform interventional procedures, perform vascular and non-vascular procedures, and other specialized applications, including angiographic studies.
Product code: JAA System, X-Ray, Fluoroscopic, Image-Intensified
Reason for recall: The Precision MPi collimator did not contain a label identifying the device as being certified to comply with applicable requirements of the x-ray performance standard.
Root cause tag: labeling and UDI
FDA root cause: Radiation Control for Health and Safety Act
Action: GE Field Engineers visited affected customers to make the correction.
Quantity in commerce: 54 (24 US / 30 OUS)
Distribution: Within the US to include: CA, CO, FL, IN, MA, MN, NV, NY, OR, PA, TN, VT, WA, and WI. OUS to include: CANADA, GERMANY, ITALY, POLAND, SAUDI ARABIA, SLOVAKIA, SPAIN, TURKEY, and UNITED KINGDOM,
Product codes and lots: serial numbers: 507001, 507002, 507003, 507004, 507005, 507006, 507007, 507008, 510001, 510002, 510003, 510004, 510005, 510006, 510007, 510008, 510009, 510010, 513001, 513002, 513004, 513005, 513006, 513007, 513008, 513009, 513010, 513011, 518002, 518003, 518004, 518005, 518006, 518007, 518008, 518009, 518010, 518011, 518012, 518013, 518014, 518015, 518016, 518017, 518018, 518019, 518020, 522001, 522002, 522003, 522004, 522005, 522006, and 522008.

Product code JAA

K033486Class IIGe Precision MpiNrt-Nordisk Rontgen Teknik A/S / cleared 2003-11-19

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)