PlainRecalls

Dorel Juvenile Group USA Recalls Inclined Sleepers Due to Safety Concerns About Inclined Sleep Products

Reported: July 31, 2019 Initiated: July 31, 2019 #19177 About 24,000 units

Dorel China, of China issued this CPSC recall on July 31, 2019. Classified as Moderate severity. Approximately About 24,000 units are affected. The recall was issued because: Infant fatalities have been reported while using other inclined sleep products, after the infants rolled from their bac…. This recall notice is sourced from official CPSC enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.

Recall Insight

This CPSC action (record #19177) was formally reported on July 31, 2019. It is classified under Moderate severity, with a current status of Active. Dorel China, of China is listed as the recalling firm. Federal records indicate About 24,000 units are affected.

The documented reason for this recall is: Infant fatalities have been reported while using other inclined sleep products, after the infants rolled from their back to their stomach or side while unrestrained, or under other circumstances. Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. The remedy documented by the agency is: Consumers should immediately stop using the inclined sleepers and contact Dorel for a refund in the form of a $60 voucher. — consumers holding this product should act on that instruction rather than relying on general guidance.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by CPSC. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 7 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.

Recall Distribution by Severity Class

Severity1Class I (Critical)Class II (Moderate)Class III (Low)
Recall Distribution by Severity Class

Severity

Moderate

Units Affected

About 24,000

Related Recalls

6

6 from same agency

Product Description

This recall involves the Eddie Bauer Slumber and Soothe Bassinet with model number BT055CSY and the Disney Baby Doze and Dream Bassinet with model number BT071DHS. The model numbers are located on a label on the underneath side of the fabric of the inclined sleeper pad. The inclined sleepers are rectangular shaped with a soft bottom, cushioned fabric, stand approximately two feet off the floor and are designed for sleeping or napping infants from birth to six months of age. The Eddie Bauer Slumber and Sooth Bassinet is beige. The Disney Baby Doze and Dream Bassinet is purple.

Reason for Recall

Infant fatalities have been reported while using other inclined sleep products, after the infants rolled from their back to their stomach or side while unrestrained, or under other circumstances.

Remedy

Consumers should immediately stop using the inclined sleepers and contact Dorel for a refund in the form of a $60 voucher.

Recall Profile

Structured summary of the CPSC recall record
Attribute Value
Agency U.S. Consumer Product Safety Commission
Severity class Moderate
Status Active
Recall number 19177
Date reported July 31, 2019
Date initiated July 31, 2019
Recalling firm Dorel China, of China
Units affected About 24,000
Distribution Not disclosed

Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.

Scale of Impact

About 24,000 units affected — limited or regional distribution scale.

Regional (<10K units)
Multi-state (10K – 100K units) ✓ This recall
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. Consumer Product Safety Commission filings.

Frequently Asked Questions

What product was recalled?
This recall involves the Eddie Bauer Slumber and Soothe Bassinet with model number BT055CSY and the Disney Baby Doze and Dream Bassinet with model number BT071DHS. The model numbers are located on a label on the underneath side of the fabric of the inclined sleeper pad. The inclined sleepers are rectangular shaped with a soft bottom, cushioned fabric, stand approximately two feet off the floor and are designed for sleeping or napping infants from birth to six months of age. The Eddie Bauer Slumber and Sooth Bassinet is beige. The Disney Baby Doze and Dream Bassinet is purple.. Recalled by Dorel China, of China. Units affected: About 24,000.
Why was this product recalled?
Infant fatalities have been reported while using other inclined sleep products, after the infants rolled from their back to their stomach or side while unrestrained, or under other circumstances.
What should consumers do?
Consumers should immediately stop using the inclined sleepers and contact Dorel for a refund in the form of a $60 voucher.
Which agency issued this recall?
This recall was issued by the CPSC on July 31, 2019. Severity: Moderate. Recall number: 19177.
How do I check if my product is affected by a recall?
Check the product description and recall number (19177) against your product. Visit the official CPSC website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
How do I report an injury from a recalled product?
Report injuries to the issuing agency: CPSC at SaferProducts.gov, NHTSA at nhtsa.gov/report-a-safety-problem, or FDA via MedWatch. Document the product (photos, model/serial numbers, purchase receipts) and seek medical attention. Injury reports help agencies track hazard patterns and may strengthen enforcement actions.

Recall Context

Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.

Nearby Recalls in This Category

Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.

Compare this recall with Infant Walkers Recalled Due to Risk of Serious Injury or De… →

Data Sources

Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
  • Source: USDA FSIS — Food Safety and Inspection Service (meat, poultry, and egg product recalls)

Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.

All federal data sources used on this page

Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).