PlainRecalls

HALO Dream Recalls Magic Sleepsuits Due to Choking Hazard

Reported: March 5, 2026 Initiated: March 5, 2026 #26315 About 45,000 units

CPSC recall on March 5, 2026. Classified as Moderate severity. Approximately About 45,000 units are affected. The recall was issued because: The zipper head can detach from certain sleepsuits, posing a choking hazard to infants.. 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 #26315) was formally reported on March 5, 2026. It is classified under Moderate severity, with a current status of Active. The recalling firm is not specified in the federal record. Federal records indicate About 45,000 units are affected.

The documented reason for this recall is: The zipper head can detach from certain sleepsuits, posing a choking hazard to infants. 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 stop using the recalled HALO Magic Sleepsuit immediately and go to the firm's website at http://www.sleepsuitrecall.com to participate in the recall. After registering, consumers wil… — 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. Because this recall is recent, remedy windows and replacement inventory are most likely still actively available from the firm or retailer. 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 45,000

Related Recalls

6

6 from same agency

Product Description

This recall involves HALO Magic Sleepsuit with batch codes PO30592, PO30641 and PO30685. The recalled infant sleepsuit shell and lining are made from 100% cotton and the fill is made from 100% polyester. It has double zippers running down each side of the front of the garment. It was sold in a variety of colors in small and large sizes. "HALO Magic Sleepsuit" is printed on the front of the sleepsuit. The batch codes and "Made in India" are printed on the sewn-in label inside the garment and the hang tag affixed to the outside of the sleepsuit.

Reason for Recall

The zipper head can detach from certain sleepsuits, posing a choking hazard to infants.

Remedy

Consumers should stop using the recalled HALO Magic Sleepsuit immediately and go to the firm's website at http://www.sleepsuitrecall.com to participate in the recall. After registering, consumers will receive a coupon code that can be applied towards a replacement sleepsuit or a $50 store credit to purchase another item on the firm's website. Do not discard the recalled garment until you have received the coupon code.

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 26315
Date reported March 5, 2026
Date initiated March 5, 2026
Recalling firm Not disclosed
Units affected About 45,000
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 45,000 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 HALO Magic Sleepsuit with batch codes PO30592, PO30641 and PO30685. The recalled infant sleepsuit shell and lining are made from 100% cotton and the fill is made from 100% polyester. It has double zippers running down each side of the front of the garment. It was sold in a variety of colors in small and large sizes. "HALO Magic Sleepsuit" is printed on the front of the sleepsuit. The batch codes and "Made in India" are printed on the sewn-in label inside the garment and the hang tag affixed to the outside of the sleepsuit.. Units affected: About 45,000.
Why was this product recalled?
The zipper head can detach from certain sleepsuits, posing a choking hazard to infants.
What should consumers do?
Consumers should stop using the recalled HALO Magic Sleepsuit immediately and go to the firm's website at http://www.sleepsuitrecall.com to participate in the recall. After registering, consumers will receive a coupon code that can be applied towards a replacement sleepsuit or a $50 store credit to purchase another item on the firm's website. Do not discard the recalled garment until you have received the coupon code.
Which agency issued this recall?
This recall was issued by the CPSC on March 5, 2026. Severity: Moderate. Recall number: 26315.
How do I check if my product is affected by a recall?
Check the product description and recall number (26315) 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.

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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).