PlainRecalls
ModerateClass IITerminated

FDA Devices recall · Reported August 15, 2018

VitalGo Total Lift Bed VG-TLB425T-TQR, Version 71064V0-27003

Potential for unintentional movement of the support surface of the bed from tilted position to horizontal position or any position in between.

Recall #
Z-2739-2018
Affected scope
85 units
Initiated
April 12, 2018
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Vitalgo Inc. recalled VitalGo Total Lift Bed VG-TLB425T-TQR, Version 71064V0-27003 - a moderate-severity action.

VitalGo Total Lift Bed VG-TLB425T-TQR, Version 71064V0-27003 was recalled by Vitalgo Inc. in August 15, 2018. Reason: Potential for unintentional movement of the support surface of the bed from tilted position to horizontal pos…. Check the official notice for the remedy. Verify recall #Z-2739-2018 with the FDA Devices before acting.

The recall

Vitalgo Inc. issued this moderate-severity FDA Devices recall-Potential for unintentional movement of the support surface of the bed from tilted position to horizontal pos….

Moderate
severity level
85 units
affected scope
Class II
classification
August 15, 2018
reported

Sourced from official FDA Devices enforcement records. Verify recall #Z-2739-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) 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.

Medical Devices recalls over time

Where this recall sits in its category - 41,021 medical devices recalls on record

01,0002,0003,0004,000 20052008201120142017202020232026 1,947
Severity1906864652High severity (most serious)Moderate severityLow severity
Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 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.

Product description

VitalGo Total Lift Bed VG-TLB425T-TQR, Version 71064V0-27003

Reason for recall

Potential for unintentional movement of the support surface of the bed from tilted position to horizontal position or any position in between.

Recall Profile

Structured summary of the FDA Devices recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Terminated
Recall number Z-2739-2018
Date reported August 15, 2018
Date initiated April 12, 2018
Recalling firm Vitalgo Inc.
Firm location Fort Lauderdale, FL
Affected scope 85 units
Distribution US distribution to Texas.

Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

85 units units affected - limited or regional distribution scale.

Regional (<10K units) ✓ This recall
Multi-state (10K – 100K units) -
Large-scale (100K – 1M units) -
Massive (≥1M units) -

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (Z-2739-2018) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Devices before acting, recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

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.

Frequently Asked Questions

What product was recalled?
VitalGo Total Lift Bed VG-TLB425T-TQR, Version 71064V0-27003. Recalled by Vitalgo Inc.. Units affected: 85 units.
Why was this product recalled?
Potential for unintentional movement of the support surface of the bed from tilted position to horizontal position or any position in between.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 15, 2018. Severity: Moderate. Recall number: Z-2739-2018.
Where was the recalled product distributed?
Distribution: US distribution to Texas..
Should I stop using a recalled medication or medical device?
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

Nationwide recalls with similar severity or category timing

Drug and device notices outside this firm and state, matched by severity timing and product category.

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This recall: FDA Devices, reported August 15, 2018. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026