The Recall Desk
Agency classClass IIOur severity:HighFDA (Devices)·Z-1499-2022·Announced 2022-08-10

Craftmatic Model 1 Adjustable Bed Base Recalled for Separation Risk

Craftmatic Industries is recalling the Model 1 Base for Dual Bed Configurations due to a potential for the bed bases to separate or slip apart. This defect could cause dual-configured beds to shift unexpectedly.

The agency’s classification

FDA (Devices): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 3/5 (High).

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: This FDA Class II recall involves a structural defect in an adjustable bed frame that could result in separation of dual bed bases. Although no injuries or illnesses have been reported and the hazard is described as potential rather than actual, it meets the rubric criterion for risk-of-harm products where injury has not yet been reported.

Plain-English summary

Craftmatic Industries, Inc. is recalling the Craftmatic Model 1 Base for Dual Bed Configurations, an adjustable bed base designed for dual bed setups. Affected model codes are 4AM663, 4AM669, 4AR391, 4AR445, 4AR797, 4AR790, and 4AR795. The product was distributed nationwide throughout the United States.

The recalled beds present a potential for the dual-configured bed bases to separate or slip away from one another during use. This defect could cause the two bases to shift apart unexpectedly, creating a gap or instability between them.

The recalled product

Product
Craftmatic Model 1 Base for Dual Bed Configurations

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (7)

  • 4AM663
  • 4AM669
  • 4AR391
  • 4AR445
  • 4AR797
  • 4AR790
  • 4AR795

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 2 recalled by Craftmatic Industries, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 2 products in this recall →

Same manufacturer · Craftmatic Industries, Inc.

See all →

Similar recalls