Recall events
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Event 69450
Event summary
Timeline bucket December 05, 2014
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording Invacare Corporation
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
G- Series Beds; G29 full length bed rails assembly
Z-1036-2015
Recall number Z-1036-2015
Initiated December 05, 2014
Classification Class II
Status Terminated
Quantity 2499 units
App-derived interpretation
Potency or specification failure
reason.potency_specification_failure · v1.0.0
out of specification
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1036-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[14333]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Invacare identified that the rail mounting bracket on the G29 full length bed rail was out of specification for entrapment safety.
Code information Model G5510 Date codes: 40121 40122 40130 40131 40201 40204 40205 40206 40210 40211 40212 40213 40214 40217 40218 40219 40220 40221 40224 40225 40226 40227 40228 40303 40304 40305 40306 40307 40310 40311 40312 40313 40314 40319 40325 40326 40327 40331 40401 40402 40403 40404 40410 40411 40414 40415 40416 40421 40422 40423 40424 40425 40429 40429 40430 40501 40502 40506 40507 40508 40512 40513 40514 40515 40516 40519 40520 40521 40522 40523 40526 40527 40528 40529 40530 40603 40604 40605 40606 40610 40611 40612 40613 40616 40617 40618 40619 40620 40623 40624 40625 40626 40627 40630 40701 40702 40703 40707 40708 40709 40714 40715 40716 40717 40721 40722 40723 40724 40728 40729 40730 40731 40805 40806 40807 40811 40812 40813 40818 40819 40820 40825 40826 40901 40902 40904
Distribution pattern US Nationwide Distribution including OH, CO, MO, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[18554]
FDA event record
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