Fresh Recalls

FDAClass II · Medical device · Recall Z-2910-2026 · Recalled August 12, 2026

Blom-Singer Classic Indwelling Voice Prosthesis recall — Freudenberg Medical, LLC

Agency report date: August 12, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Blom-Singer Classic Indwelling Voice Prosthesis
Company / brand
Freudenberg Medical
Lot / serial / date codes
Lot #0000369205/UDI: 00813307014232
Distribution
US Nationwide distribution in the states of IN, OH, AZ, WA, FL, MO, KY, IN, NY and the countries of GBR, FRA.
Agency product description and boundaries

Blom-Singer Classic Indwelling Voice Prosthesis, 16Fr/10 mm REF: 1610-LF

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Incorrect labeling- The labeled box for the Large Esophageal Flange contains a Large Esophageal and Tracheal Flange, and the labeled box for the Large Esophageal and Tracheal Flange contains a Large Esophageal Flange.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Blom-Singer Classic Indwelling Voice Prosthesis

3. Open the official notice or contact

Official recall ID
Z-2910-2026
Brand
Freudenberg Medical
Classification
Class II
Units affected
40 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Carpinteria, CA, United States
Firm address
1110 Mark Ave, 93013-2918

Identifying details (verbatim from the notice)

Product codes / lots
Lot #0000369205/UDI: 00813307014232
Distribution
US Nationwide distribution in the states of IN, OH, AZ, WA, FL, MO, KY, IN, NY and the countries of GBR, FRA.
Firm notified the public via
Letter
FDA event ID
99299
Recall initiated
June 17, 2026
FDA classified
August 6, 2026
FDA report date
August 12, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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