Fresh Recalls

FDAClass I · Drug · Recall D-0620-2026 · Recalled June 17, 2026

BEEKEEPER'S NATURALS Saline Nasal Spray recall — BEEKEEPER'S NATURALS USA INC.

Agency report date: June 17, 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
BEEKEEPER'S NATURALS Saline Nasal Spray
Company / brand
BEEKEEPER'S NATURALS USA
Lot / serial / date codes
Lot #: 5950, Exp. Date 02/2028
Distribution
Nationwide within the United States.
Agency product description and boundaries

BEEKEEPER'S NATURALS Saline Nasal Spray, Sinus Congestion Rinse, Made with Propolis + Xylitol, 1 FL OZ (30 mL) per bottle, Manufactured For: Beekeeper's Naturals USA Inc., Covina, CA 91789.

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: Microbial Contamination of Non-Sterile Products

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

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: BEEKEEPER'S NATURALS Saline Nasal Spray

3. Open the official notice or contact

Official recall ID
D-0620-2026
Brand
BEEKEEPER'S NATURALS USA
Classification
Class I
Units affected
1680 bottles
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Covina, CA, United States
Firm address
440 N Barranca Ave # 9223, N/A, 91723-1722

Identifying details (verbatim from the notice)

Product codes / lots
Lot #: 5950, Exp. Date 02/2028
Distribution
Nationwide within the United States.
Firm notified the public via
Letter
FDA event ID
99145
Recall initiated
June 1, 2026
FDA classified
June 24, 2026
FDA report date
June 17, 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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