Severity
Moderate
FDA Devices recall · Reported November 5, 2014
The Easy-Care Care-Lock feature installed at the foot of the bed may potentially fail to stay engaged (locked) after the Care-Lock System has been engaged by stepping on the red (…
Joerns Healthcare recalled Joerns EasyCare Bed Product Usage: The AC-powered adjustable hospital bed is a device… - a moderate-severity action.
Joerns EasyCare Bed Product Usage: The AC-powered adjustable hospital bed is a device… was recalled by Joerns Healthcare in November 5, 2014. Reason: The Easy-Care Care-Lock feature installed at the foot of the bed may potentially fail to stay engaged (locked…. Check the official notice for the remedy. Verify recall #Z-0151-2015 with the FDA Devices before acting.
The recall
Joerns Healthcare issued this moderate-severity FDA Devices recall-The Easy-Care Care-Lock feature installed at the foot of the bed may potentially fail to stay engaged (locked….
Sourced from official FDA Devices enforcement records. Verify recall #Z-0151-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Devices action (record #Z-0151-2015) was formally reported on November 5, 2014, with the manufacturer initiating the action on September 24, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. Joerns Healthcare is listed as the recalling firm, operating out of Arlington, TX. Federal records list the affected scope as 3135.
The documented reason for this recall is: The Easy-Care Care-Lock feature installed at the foot of the bed may potentially fail to stay engaged (locked) after the Care-Lock System has been engaged by stepping on the red (locked) pedal. Distribution data in the federal record shows the product reached: Worldwide Distribution: US (nationwide) and country of: Canada.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 40,861 medical devices recalls on record
Of 88,001 recalls with an agency hazard classification, 19,020 are high severity, 64,468 moderate, and 4,513 low. A further 16,157 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
3135
Related Recalls
6
6 from same agency
Joerns EasyCare Bed Product Usage: The AC-powered adjustable hospital bed is a device intended for medical purposes. The bed includes a built-in electric motor and remote controls that can be operated by the patient to adjust the height and surface contour of the bed.
The Easy-Care Care-Lock feature installed at the foot of the bed may potentially fail to stay engaged (locked) after the Care-Lock System has been engaged by stepping on the red (locked) pedal.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0151-2015 |
| Date reported | November 5, 2014 |
| Date initiated | September 24, 2014 |
| Recalling firm | Joerns Healthcare |
| Firm location | Arlington, TX |
| Affected scope | 3135 |
| Distribution | Worldwide Distribution: US (nationwide) and country of: Canada. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Two federal-filing-derived peer sets for this notice, both outside the same recalling firm and filing state so the neighborhoods are not firm or geographic containment.
Same archive severity grade (Moderate), closest by report date among other firms and states.
Same product category, closest by report date among other firms and states (deduped against the severity set).
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported November 5, 2014. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.