PlainRecalls

Philips Avent Digital Video Baby Monitors Recalled by Philips Personal Health Due to Burn Hazard

Reported: August 3, 2023 Initiated: August 3, 2023 #23250 About 12,850 units

Philips Consumer Lifestyle B.V., of The Netherlands issued this CPSC recall on August 3, 2023. Classified as Moderate severity. Approximately About 12,850 units are affected. The recall was issued because: The rechargeable lithium-ion batteries in the Parent Unit monitors can overheat during charging, posing a risk of burns…. 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 #23250) was formally reported on August 3, 2023. It is classified under Moderate severity, with a current status of Active. Philips Consumer Lifestyle B.V., of The Netherlands is listed as the recalling firm. Federal records indicate About 12,850 units are affected.

The documented reason for this recall is: The rechargeable lithium-ion batteries in the Parent Unit monitors can overheat during charging, posing a risk of burns and property damage. 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 Digital Video Baby Monitors and contact Philips Avent for a free replacement. — 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. 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 3 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 12,850

Related Recalls

6

0 from same agency

Product Description

This recall involves Philips Avent video baby monitors used to remotely monitor infants. They consist of a Baby Unit (camera) and a Parent Unit (monitor) pair. The monitor has a 3.5-inch color screen. The recalled baby monitors include models SCD630 and SCD843 only, manufactured between March 2016 and December 2019. The model numbers and production date codes, in day-month-year format, are located on the bottom of the Parent Unit. The monitors and camera are white. Philips Avent is printed on the front.

Reason for Recall

The rechargeable lithium-ion batteries in the Parent Unit monitors can overheat during charging, posing a risk of burns and property damage.

Remedy

Consumers should immediately stop using the Digital Video Baby Monitors and contact Philips Avent for a free replacement.

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 23250
Date reported August 3, 2023
Date initiated August 3, 2023
Recalling firm Philips Consumer Lifestyle B.V., of The Netherlands
Units affected About 12,850
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 12,850 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 Philips Avent video baby monitors used to remotely monitor infants. They consist of a Baby Unit (camera) and a Parent Unit (monitor) pair. The monitor has a 3.5-inch color screen. The recalled baby monitors include models SCD630 and SCD843 only, manufactured between March 2016 and December 2019. The model numbers and production date codes, in day-month-year format, are located on the bottom of the Parent Unit. The monitors and camera are white. Philips Avent is printed on the front.. Recalled by Philips Consumer Lifestyle B.V., of The Netherlands. Units affected: About 12,850.
Why was this product recalled?
The rechargeable lithium-ion batteries in the Parent Unit monitors can overheat during charging, posing a risk of burns and property damage.
What should consumers do?
Consumers should immediately stop using the Digital Video Baby Monitors and contact Philips Avent for a free replacement.
Which agency issued this recall?
This recall was issued by the CPSC on August 3, 2023. Severity: Moderate. Recall number: 23250.
How do I check if my product is affected by a recall?
Check the product description and recall number (23250) 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 Endo-Model Replacement Plateau; Item Number: 15-0027/11; →

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).