BEEKEEPER'S NATURALS Saline Nasal Spray, 30 mL recall — Beekeeper's Naturals Usa Inc. (Class I)

Beekeeper's Naturals Usa Inc. is recorded by the U.S. Food and Drug Administration (FDA) as recalling BEEKEEPER'S NATURALS Saline Nasal Spray, 30 mL — a Class I recall, initiated 2026-06-01 and posted to the FDA enforcement report on 2026-06-17, under recall number D-0620-2026. Status Ongoing, with no termination date on the record. The reason the FDA record carries is, verbatim: “Microbial Contamination of Non-Sterile Products”. From the product description, the form is nasal spray, the strength given is 30 mL and the package is described as 1 FL OZ (30 mL). Distribution is recorded as “Nationwide within the United States” — Nationwide (US), with the recalling firm on record in CA, United States. It is the only recall number the FDA has filed under event ID 99145. 16 days separate the firm's initiation date from the FDA's report date on this record. Values are reproduced from the linked openFDA report; regulatory information, not medical advice.

Regulatory snapshot

Recall number D-0620-2026
FDA event ID 99145
Classification Class I (most serious regulatory tier)
Status Ongoing
Recalling firm Beekeeper's Naturals Usa Inc.
Recall initiated 2026-06-01
Reported by FDA 2026-06-17
Report lag 16 days from initiation to report
Distribution Nationwide within the United States. — Nationwide (US)
Firm location on record CA, United States
Product description (source) 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.

Reason reported by FDA

Microbial Contamination of Non-Sterile Products

5 words from the enforcement report field reason_for_recall, reproduced without edit — the firm's own wording, not an assessment.

Product identifiers in this record

4 identifying values matched by exact pattern in the 29-word product description above; each is a literal substring of it.

Product named BEEKEEPER'S NATURALS Saline Nasal Spray
Form Nasal Spray
Strength 30 mL
Package 1 FL OZ (30 mL)
Manufactured for Beekeeper's Naturals USA Inc., Covina

Reported in the same month (2026-06)

74 enforcement reports carry a report date in 2026-06; these 2 are the Class I ones nearest this record.

Recall recordRecall numberRecalling firmFDA tierReported
DOXOrubin Hydrochloride Liposome injection, 50 mg/25 mLD-0580-2026Sun Pharmaceutical Industries IncClass I2026-06-17
Gas-X Extra Strength, 125 mgD-0595-2026Haleon US Holdings LLCClass I2026-06-17

Nearest Class I recalls by date

11 of 250 indexed records share the Class I tier; the 8 nearest to 2026-06-17 by report date are listed here.

Recall recordRecall numberRecalling firmStrength / formReported
BD ChloraPrep Clear, 2%D-0624-2026Carefusion 213, LLC2% · Solution2026-07-01
BD ChloraPrep FREPP Clear, 2%D-0625-2026Carefusion 213, LLC2% · Solution2026-07-01
MG217 Multi-Symptom Treatment Cream & Skin Protectant (colloidal oatmeal 2%)D-0553-2026Wisconsin Pharmacal Company2% · Cream2026-05-27
Revitaderm Wound Care Gel, 0.1%D-0692-2026Blaine Labs Inc0.1% · Gel2026-07-08
Lactated Ringer's Injection USP, 1000 mLD-0540-2026B Braun Medical Inc1000 mL · Injection2026-05-13
Cetirizine Hydrochloride Tablets USP 5 mgD-0732-2026JB Chemicals And Pharmaceuticals Ltd5 mg · Tablets2026-07-29
Cyclophosphamide for Injection, 1 gram/vialD-0743-2026Sunny Pharmtech Inc.1 gram/vial · for Injection2026-08-12
Cyclophosphamide for Injection, 2 gram/vialD-0744-2026Sunny Pharmtech Inc.2 gram/vial · for Injection2026-08-12

Reading this record

Class I is the FDA's own severity tier for the recall action — 11 of the 250 indexed records carry it — and it describes the agency's assessment of the action, not a risk statement about any individual.

Namespace context: the Class I index (11 records) and the recall hub (250 records, 118 FDA events); Beekeeper's Naturals Usa Inc. (1 indexed records) aggregates this firm across datasets.

Coverage and limits of this record

This page reflects the openFDA enforcement report for D-0620-2026 as ingested on 2026-08-22, which can lag the live FDA record and omits detail held only in primary documents. It offers no clinical assessment, no advice about whether to use any product, and no substitute. For any health question consult a qualified healthcare professional.

Source & provenance

Official source
https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0620-2026%22
Source dataset
openFDA Drug Enforcement API
Publication date
2026-06-17
Ingested
2026-08-22
Record hash
12948e968af97114

Verify every value against the official FDA source above. This site links to the regulator's record rather than replacing it.