PlainRecalls

Bose Recalls EdgeMax® and FreeSpace® Loudspeakers Due to Injury Hazard (Recall Alert)

Reported: July 10, 2019 Initiated: July 10, 2019 #19760 About 77,500 units

CPSC recall on July 10, 2019. Classified as Moderate severity. Approximately About 77,500 units are affected. The recall was issued because: The loudspeaker's mounting components can break causing the speakers to dislodge and fall from its installed location, …. 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 #19760) was formally reported on July 10, 2019. 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 77,500 units are affected.

The documented reason for this recall is: The loudspeaker's mounting components can break causing the speakers to dislodge and fall from its installed location, posing an injury hazard. 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: Stop using the recalled loudspeakers immediately and contact Bose for instructions on receiving a free replacement or free safety cables. Bose is contacting all known purchasers directly. — 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 77,500

Related Recalls

6

6 from same agency

Product Description

This recall involves FreeSpace DS40F in-ceiling/flush-mount loudspeakers manufactured before August 13, 2018, and all FreeSpace and EdgeMax in-ceiling/flush-mount loudspeakers installed in commercial cooking environments. The loudspeakers were sold in black and white colors with "Bose" engraved on the front of them. Model numbers and the date of manufacturing can be found on the label on the back of the loudspeaker. These professional loudspeakers were sold by Bose through authorized Bose resellers to commercial purchasers, not at retail to consumers, although affected loudspeakers may have been installed in commercial spaces open to the public. These names and model numbers are included in the recall. PRODUCT NAME PHOTO RECALLED MODEL NUMBERS/ SKUs BOSE EdgeMax EM90/EM180 (In-ceiling/Flush-mount) 777189-0210 778844-0210 BOSE FreeSpace DS 16F 352419-0210 43053 43054 52123 29384 31945 40153 29383 40152 29685 35173 29385 31946 BOSE FreeSpace DS 16S/SE 40786 40785 52092 726793-0110 726793-0210 352416-0110 352416-0210 40783 52090 40784 52091 BOSE FreeSpace DS 40F 312278-0231 321278-0251 321278-0250 321278-025R 321278-0131 321278-0120 321278-0140 321278-0220 321278-0240 321278-024R 321278-0110 321278-0130 321278-013R 321278-0210 321278-0230 321278-023R BOSE FreeSpace DS 40SE 726792-0110 726792-0210 321279-0150 321279-0250 321279-0110 321279-011R 321279-0120 321279-0220 321279-0210 321279-021R 321279-0130 321279-0230 BOSE FreeSpace DS 100F 40804 40805 52095 352421-0210 BOSE FreeSpace DS 100SE 40806 52097 40807 52098 726790-0110 726790-0210 294955-0110 294955-0210 352422-0110 352422-011R 352422-0210 BOSE FreeSpace 3 Flush-Mount Satellites 31938 31939 29827 40150 32036 29387 40149 BOSE FreeSpace 3 Series II Acoustimass (bass) 29686 40148 29386 40147 32033 31937 31936

Reason for Recall

The loudspeaker's mounting components can break causing the speakers to dislodge and fall from its installed location, posing an injury hazard.

Remedy

Stop using the recalled loudspeakers immediately and contact Bose for instructions on receiving a free replacement or free safety cables. Bose is contacting all known purchasers directly.

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 19760
Date reported July 10, 2019
Date initiated July 10, 2019
Recalling firm Not disclosed
Units affected About 77,500
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 77,500 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 FreeSpace DS40F in-ceiling/flush-mount loudspeakers manufactured before August 13, 2018, and all FreeSpace and EdgeMax in-ceiling/flush-mount loudspeakers installed in commercial cooking environments. The loudspeakers were sold in black and white colors with "Bose" engraved on the front of them. Model numbers and the date of manufacturing can be found on the label on the back of the loudspeaker. These professional loudspeakers were sold by Bose through authorized Bose resellers to commercial purchasers, not at retail to consumers, although affected loudspeakers may have been installed in commercial spaces open to the public. These names and model numbers are included in the recall. PRODUCT NAME PHOTO RECALLED MODEL NUMBERS/ SKUs BOSE EdgeMax EM90/EM180 (In-ceiling/Flush-mount) 777189-0210 778844-0210 BOSE FreeSpace DS 16F 352419-0210 43053 43054 52123 29384 31945 40153 29383 40152 29685 35173 29385 31946 BOSE FreeSpace DS 16S/SE 40786 40785 52092 726793-0110 726793-0210 352416-0110 352416-0210 40783 52090 40784 52091 BOSE FreeSpace DS 40F 312278-0231 321278-0251 321278-0250 321278-025R 321278-0131 321278-0120 321278-0140 321278-0220 321278-0240 321278-024R 321278-0110 321278-0130 321278-013R 321278-0210 321278-0230 321278-023R BOSE FreeSpace DS 40SE 726792-0110 726792-0210 321279-0150 321279-0250 321279-0110 321279-011R 321279-0120 321279-0220 321279-0210 321279-021R 321279-0130 321279-0230 BOSE FreeSpace DS 100F 40804 40805 52095 352421-0210 BOSE FreeSpace DS 100SE 40806 52097 40807 52098 726790-0110 726790-0210 294955-0110 294955-0210 352422-0110 352422-011R 352422-0210 BOSE FreeSpace 3 Flush-Mount Satellites 31938 31939 29827 40150 32036 29387 40149 BOSE FreeSpace 3 Series II Acoustimass (bass) 29686 40148 29386 40147 32033 31937 31936. Units affected: About 77,500.
Why was this product recalled?
The loudspeaker's mounting components can break causing the speakers to dislodge and fall from its installed location, posing an injury hazard.
What should consumers do?
Stop using the recalled loudspeakers immediately and contact Bose for instructions on receiving a free replacement or free safety cables. Bose is contacting all known purchasers directly.
Which agency issued this recall?
This recall was issued by the CPSC on July 10, 2019. Severity: Moderate. Recall number: 19760.
How do I check if my product is affected by a recall?
Check the product description and recall number (19760) 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).