Z-1865-2012Class II

OEC Uroview 2800, Model number A349855. Designed to provide fluoroscopic and spot-film imaging of the patient...

Name: Z-1865-2012 OEC Uroview 2800, Model number A349855. Designed to provide fluoroscopic and spot-film imaging of the patient...
Creator: GE OEC Medical Systems, Inc
Published: 2006-11-20
License: https://open.fda.gov/license/

GE Healthcare / initiated 2006-11-20 / Terminated / root cause: software

FDA source

GE OEC Medical Systems, Inc began a recall of OEC Uroview 2800, Model number A349855. Designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical, and interventional... on 2006-11-20. FDA classified it as Class II and gives the reason as "Recalled in November 2006 due to several intermittent potential safety issues including navigation tracking inaccuracy, system Lok-up, incorrect image display, incorrect dose area calculated air kerma in "film mode" and...". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as software.

Recall record

Recall number: Z-1865-2012
Classification: Class II
Status: Terminated
Initiated: 2006-11-20
Posted: 2012-06-22
Terminated: 2012-06-25
Recalling firm: GE Healthcare
Product: OEC Uroview 2800, Model number A349855. Designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical, and interventional procedures.
Product code: JAA System, X-Ray, Fluoroscopic, Image-Intensified
Reason for recall: Recalled in November 2006 due to several intermittent potential safety issues including navigation tracking inaccuracy, system Lok-up, incorrect image display, incorrect dose area calculated air kerma in "film mode" and "digital spot mode", and the system does not reboot.
Root cause tag: software
FDA root cause: Software design
Action: On 11/20/06 two written notifications were sent to consignees addressed to the Facility Administrator and the Radiology Administrator. The notifications advised them that GE Healthcare had identified several intermittent potential safety issues that may occur with the product. Interim solutions were provided for each issue. The letter stated that GEHC OEC would contact customers and remedy the issues free of charge when a permanent solution became available. An Urgent Recall Notice, dated April 13, 2007, was also sent to customers. Customers were to contact the service team at 800-874-7378 for further information, if there were any questions or concerns.
Quantity in commerce: 717 units
Distribution: Worldwide Distribution.
Product codes and lots: All Serial Numbers: P4-0004-L , P4-0005-L , P4-0006-R-RC1 , P4-0008-R , P4-0011-L , P6-0654-R , P4-0012-R , P4-0013-L , P4-0014-L , P4-0015-L , P4-0016-L , P4-0017-L , P4-0018-L , P4-0019-R , P4-0020-L , P4-0021-L , P4-0022-R , P4-0023-L , P4-0024-R , P4-0025-R , P4-0026-L , P4-0027-R , P4-0028-R , P4-0029-R , P4-0030-R , P4-0031-L , P4-0680-L , P4-0032-R , P4-0033-R , P4-0034-R , P4-0035-R , P4-0036-R , P4-0037-R , P4-0038-L , P4-0039-R , P4-0042-R , P4-0044-L , P4-0045-R , P4-0046-L , P4-0047-L-RC , P4-0048-L , P4-0049-R , P4-0050-L , P4-0051-L , P4-0052-R , P4-0053-L , P4-0054-R , P4-0074-R , P4-0055-L , P4-0058-R , P4-0059-L , P4-0062-L , P4-0064-L , P4-0067-L , P4-0075-L , P4-0068-R , P4-0070-L , P4-0071-L , P4-0073-R , P4-0076-R , P4-0078-R , P4-0081-L , P4-0082-R , P4-0388-L , P4-0084-R , P4-0085-R , P4-0087-R , P4-0088-L , P4-0089-L , P4-0090-L , P4-0092-R , P4-0093-R , P4-0094-R , P4-0095-R , P4-0097-R , P4-0098-R , P4-0099-L , P4-0100-R , P4-0101-R , 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P4-0523-R , P4-0524-L , P4-0531-R , P4-0532-R , P4-0537-L , P4-0539-L , P4-0540-L , P4-0541-L , P4-0545-L , P4-0548-L , P4-0550-L , P4-0551-L , P4-0560-R , P4-0561-L , P4-0566-L , P4-0569-R , P4-0570-R , P4-0573-R , P4-0574-R , P4-0575-L , P4-0576-L , P4-0581-R , P4-0588-R , P4-0589-L , P4-0590-R , P4-0591-R , P4-0592-R , P4-0594-L , P4-0595-L , P4-0596-L , P4-0597-R , P4-0602-L , P4-0603-R , P4-0605-R , P4-0607-L , P4-0608-R , P4-0611-L , P4-0613-R , P4-0615-L , P4-0616-R , P4-0626-R , P4-0628-L , P4-0631-L , P4-0633-L , P4-0636-R , P4-0637-R , P4-0638-R , P4-0639-R , P4-0640-R , P4-0641-R , P4-0642-R , P4-0644-L , P4-0645-R , P4-0648-L , P4-0650-L , P4-0652-L , P4-0653-L , P4-0655-R , P4-0656-R , P4-0657-L , P6-0598-L , P4-0662-L , P4-0666-L , P4-0668-R , P4-0669-R , P4-0670-R , P4-0679-R , P4-0686-L , P4-0694-R , P4-0701-R , P4-0702-R , P4-0717-L , P4-0723-R , P4-0730-L , P6-0040-R , P6-0043-R, P6-0214-R, P6-0219-L, P6-0220-L, P6-0221-R, P6-0222-R,P6-0225-R, P6-0227-R, P6-0230-L, P6-0249-R, P6-0251-L, P6-0252-L , P6-0253 , P6-0056-L , P6-0061-L-RC , P6-0066-R , P6-0069-R , P6-0072-R , P6-0077-R , P6-0079-L , P6-0080-L , P6-0083-L , P6-0091-R , P6-0096-R , P6-0106-R , P6-0109-L , P6-0116-R , P6-0122-L , P6-0125-R , P6-0126-L , P6-0582-L , P6-0129-R , P6-0130-R , P6-0134-R, P6-0144-L , P6-0182-L , P6-0135-L , P6-0136-R , P6-0137-R , P6-0139-R , P6-0145-L , P6-0148-R-RC , P6-0150-L , P6-0152-L , P6-0156-L , P6-0157-R , P6-0166-L , P6-0171-L , P6-0184-L , P6-0186-R , P6-0192-L , P6-0193-R , P6-0198-L , P6-0200-R , P6-0210-L , P6-0213-L , P6-0218-R , P6-0226-R , P6-0228-R , P6-0229-R , P6-0231-L , P6-0233-L , P6-0234-R , P6-0235-R , P6-0699-R , P6-0236-R , P6-0243-L , P6-0245-L , P6-0250-R , P6-0261-R , P6-0262-R , P6-0265-L , P6-0267-R , P6-0270-L-RC , P6-0709-R , P6-0275-L , P6-0276-L , P6-0278-R , P6-0283-R , P6-0286-R , P6-0287-L , P6-0290-R , P6-0291-L , P6-0295-R , P6-0303-L , P6-0307-L , P6-0311-R , P6-0312-L , P6-0314-L , P6-0317-R , P6-0320-R , P6-0324-R , P6-0330-L , P6-0336-L , P6-0338-L , P6-0344-R , P6-0351-L , P6-0704-L , P6-0352-R , P6-0358-R , P6-0360-L , P6-0363-L , P6-0364-L , P6-0366-R , P6-0371-R , P6-0372-R , P6-0375-L , P6-0378-L , P6-0383-R , P6-0387-L , P6-0392-R , P6-0397-L , P6-0398-L , P6-0399-L , P6-0412-R , P6-0414-R , P6-0420-R , P6-0421-R , P6-0423-R , P6-0427-L , P6-0432-R , P6-0435-R , P6-0437-R , P6-0438-R , P6-0439-L , P6-0461-L , P6-0462-R , P6-0468-L , P6-0470-R , P6-0479-R , P6-0480-R , P6-0486-R , P6-0493-R , P6-0494-R , P6-0497-R , P6-0499-R , P6-0502-R , P6-0522-R , P6-0509-L , P6-0510-L , P6-0512-L , P6-0513-R , P6-0514-R , P6-0515-L , P6-0516-R , P6-0518-R , P6-0519-R , P6-0520-L , P6-0521-R , P6-0530-R , P6-0533-L , P6-0534-L , P6-0538-R , P6-0542-R , P6-0543-R , P6-0544-R , P6-0546-L , P6-0549-R , P6-0552-L , P6-0553-R , P6-0554-R , P6-0555-L , P6-0558-L , P6-0559-L , P6-0562-R , P6-0563-R , P6-0564-R , P6-0565-R , P6-0567-R , P6-0571-L , P6-0572-L , P6-0577-R , P6-0578-R , P6-0579-R , P6-0583-R , 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Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1865-2012
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1865-2012	Class II	Terminated	FDA Mandated	2012-07-04	2012-06-22

Product code JAA

K993687Class IIUroview 2800Ge Dec Medical Systems / cleared 1999-12-21

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 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)