FDA Device recall Z-1607-2015

Nuclear gamma cameras (ADAC VERTEX PLUS/SOLUS/CARDIO, ADAC VERTEX V60 & ADAC CARDIO C60) Nuclear gamma cameras intended to produce images d…

FDA Device
Class II
terminated
Published 2015-05-20

On 2015-05-20 the FDA classified a Class II recall of Nuclear gamma cameras (ADAC VERTEX PLUS/SOLUS/CARDIO, ADAC VERTEX V60 & ADAC CARDIO C60) Nuclear gamma cameras intended to produce images d… by Philips Medical Systems Cleveland, citing the firm was notified by a customer that the collimator exchange carriage and the collimator storage cabinet were misaligned.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1607-2015
Classification	Class II
Status	terminated
Initiated	2015-03-11
Published	2015-05-20
Last updated	2026-09-13 11:53 UTC
Company	Philips Medical Systems Cleveland
Distribution	US

Product

Nuclear gamma cameras (ADAC VERTEX PLUS/SOLUS/CARDIO, ADAC VERTEX V60 & ADAC CARDIO C60) Nuclear gamma cameras intended to produce images depicting the anatomical distribution of single photon and positron emitting radioisotopes with the human body for interpretation by medical personnel.

Reason

The firm was notified by a customer that the collimator exchange carriage and the collimator storage cabinet were misaligned.

Identifiers

code_info	VERTEX PLUS/SOLUS/CARDIO Model #88297; Serial #s: 9504103, 9703171, 9802304, 9809124, 9809415, 9810438, 9910015, 99117… VERTEX PLUS/SOLUS/CARDIO Model #88297; Serial #s: 9504103, 9703171, 9802304, 9809124, 9809415, 9810438, 9910015, 9911711, _0002032, 0007001M, 0008009B, 0011002B, 0101002C, 0102019V, 0103020V, 01069VM, 01070VM, 0111001V, 01295VM, 01296K, 01864VM, 03026VM, 0939VM, 100098-01N, 1006, 1008, 10252, 1027, 1062701, 1062701, 10630, 1092, 1097, 11, 11090, 130234-01NVERTEX, 2035, 2038, 2047, 3059, 3060, 3064, 4007, 4078, 5934V, 6052, 6090VM, 6261, 7373VM, 7376VM, 7386VM, 7560VM, 7561VM, 8002, 802080322, 85247, 9054VM/V, 9056VM/V, 9073152, 9130VM, 9205345, 940384, 9408127, 9408136, 9503084, 9504096, 9506016, 9506145, 9511123, 9512008, 9512009, 9512018, 9601012, 9601015, 9601016, 9601024, 9601036, 9602161, 9602245, 9602246, 9602254, 9603336, 9604016, 9604021, 9605024, 9605026, 9605037, 9606211, 9607015, 9607024, 9608031, 9608046, 9608049, 9608050, 9608052, 9608052, 9608064, 9609063, 9609081, 9610058, 9611003, 9611035, 9611077, 9611082, 9612072, 9701127, 9702095, 9702150, 9703154, 9703165, 9704044,

code_info

VERTEX PLUS/SOLUS/CARDIO Model #88297; Serial #s: 9504103, 9703171, 9802304, 9809124, 9809415, 9810438, 9910015, 99117…

VERTEX PLUS/SOLUS/CARDIO Model #88297; Serial #s: 9504103, 9703171, 9802304, 9809124, 9809415, 9810438, 9910015, 9911711, _0002032, 0007001M, 0008009B, 0011002B, 0101002C, 0102019V, 0103020V, 01069VM, 01070VM, 0111001V, 01295VM, 01296K, 01864VM, 03026VM, 0939VM, 100098-01N, 1006, 1008, 10252, 1027, 1062701, 1062701, 10630, 1092, 1097, 11, 11090, 130234-01NVERTEX, 2035, 2038, 2047, 3059, 3060, 3064, 4007, 4078, 5934V, 6052, 6090VM, 6261, 7373VM, 7376VM, 7386VM, 7560VM, 7561VM, 8002, 802080322, 85247, 9054VM/V, 9056VM/V, 9073152, 9130VM, 9205345, 940384, 9408127, 9408136, 9503084, 9504096, 9506016, 9506145, 9511123, 9512008, 9512009, 9512018, 9601012, 9601015, 9601016, 9601024, 9601036, 9602161, 9602245, 9602246, 9602254, 9603336, 9604016, 9604021, 9605024, 9605026, 9605037, 9606211, 9607015, 9607024, 9608031, 9608046, 9608049, 9608050, 9608052, 9608052, 9608064, 9609063, 9609081, 9610058, 9611003, 9611035, 9611077, 9611082, 9612072, 9701127, 9702095, 9702150, 9703154, 9703165, 9704044,

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1607-2015%22

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