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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 72448

1 recalled-product record grouped only because every row carries this exact official event ID.

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Event summary

Timeline bucket
September 23, 2015
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
GE Medical Systems, LLC

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 1

MR Surgical Suite II Table, Model Number(s): M8074SS, M8053SS, M0074SS. UPDATE 11-4-2015: Model M0001SS

Z-0196-2016
Recall number
Z-0196-2016
Initiated
September 23, 2015
Classification
Class II
Status
Terminated
Recalling firm
GE Medical Systems, LLC
Quantity
23 (11 US; 12 OUS) Update 11-4-2015: 35 (14 US; 21 OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
GE became aware of an issue with the table transfer release mechanism of the MR Surgical Suite Option. The issue may prevent patient transfer between the MR and surgical tables.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

GE became aware of an issue with the table transfer release mechanism of the MR Surgical Suite Option. The issue may prevent patient transfer between the MR and surgical tables.

Code information

Mfg Lot or Serial # System ID 00000304124MR1 904202MR8 00000000UA0116 330344MR750W 00000000UA0117 616267IMRI UA0326 614293MR9 00000307553MR8 415UCBHMR1 00000000UA0296 309655MR750W 00000000UA0396 713792AMR14 00000012228M63 608263MR4IOR N/A 614RMHTMR1 N/A 720848MR4 N/A 309655IMRI 00000299229MR5 AH5824MR01 00000014131M67 MRHM0323 00000018480M64 MR307144MR6 00000021158M61 MRHM0885 00000013254M68 082445160014 00001309FMM07L T4185506 DUMFMI60876024 M347028301 00000021695M62 M4194477 00000305145MR5 UC2547MR01 00001219FMM0H1 EM0105 00001105XF5047 PL2853MR01 00001251FMM044 34368MRS01 UPDATE 11-4-2015: Mfg Lot or Serial # System ID 2 602406IMR 3 507284NMRV N/A 214820ITABLE N/A 416369MR3T 000000PTST0008 082427040101 000000PTST0007 082427050024 000000PTST0003 CS1020MR01 N/A CS1006MR03 4 YM1733 000000PTST0010 YM3833 000000PTST0006 ZA2169MR01 000000PTST0005 10590MRS01

Distribution pattern

Worldwide Distribution - US Distribution including the states of : CA, CO, FL, IL, MI, OH, TX and WI., and to the countries of : AUSTRIA, BRAZIL, FRANCE, GERMANY, JAPAN, POLAND and TURKEY. UPDATE 11-4-2015: Additional states: AZ, MN. Additional countries: Canada, China, Czech Republic, South Africa, and United Kingdom