NM/CT 870 DR Product Usage: The GE Discovery NM/CT 670 recall
NM/CT 870 DR Product Usage: The GE Discovery NM/CT 670 system is a medical tool intended for use by appropriately trained health professionals to aid…
Why was NM/CT 870 DR Product Usage: The GE Discovery NM/CT 670 recalled?
During installation of certain Nuclear Medicine systems delivered with dismounted detectors, some detector screws may not have been secured correctly, leading to the possible loss of one detector mounting design redundancy.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Mfg. Lot or Serial # System ID Model, Catalogue or Code # 870Y64037 SHIPPED (GON 4566933) H3100AS 870Y64040 SHIPPED (GON 4751375) H3100AS 870X64011 216844DR870 H3100AS 870X64024 802775D870 H3100AS 870X64002 206SCCANM H3100AS 870X64032 262741NUC H3100AS 870X64001 030020NU06 H3100AS 870Y64034 514345BD870 H3100AS 870Y64035 M54606132 H3100AS 870X64012 X634445001 H3100AS 870X64007 V2728113 H3100AS 870X64009 M4016255 H3100AS 870X64026 M40230109 H3100AS 870X64017 M40240121 H3100Q 870X64018 M40240122 H3100Q 870X64016 499221NU01 H3100AS 870X64022 A5173220 H3100AS NT3DG1800003BH NS0303 5376204-70-60-1 NT3DG1800002BH NS0302 5376204-70-60-1 870X64025 EMM0530 H3100AS 870Y64038 MST01300 H3100AS 870X64029 PL1031NM01 H3100AS 870X64027 PL0398NM01 H3100AS 870X64030 PL2190NM01 H3100AS 870X64028 PL0372NM01 H3100AS 870X64013 NP473631 H3100AS 870X64008 00669NUC03 H3100AS
- Product
- NM/CT 870 DR Product Usage: The GE Discovery NM/CT 670 system is a medical tool intended for use by appropriately trained health professionals to aid…
- Recalling firm
- GE Healthcare, LLC
- Quantity
- 27 units
- Distribution
- US and Austria, Canada, Croatia, France, Germany, India, Italy, Japan, Republic of Korea, Netherlands, Poland, Portugal, Slovakia, South Africa, Spain, Sweden, Switzerland, UK
- Recall date
- May 8, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)