CLASS I Drug recall · Reported 6 Jul 2022 · FDA Enforcement Report
Allergy Bee Gone for Kids Nasal Swab Remedy tubes recalled by Buzzagogo
Buzzagogo is recalling Allergy Bee Gone for Kids Nasal Swab Remedy tubes. The recall was initiated on 8 Jun 2022 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1160-2022
- FDA event ID
- 90382
- Recalling firm
- Buzzagogo, Nottingham, NH
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 8 Jun 2022
- FDA classified
- 24 Jun 2022
- Reported
- 6 Jul 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Other Bacterial Contamination
- Drug class
- Nasal Sprays
Timeline
| 8 Jun 2022 | Recall initiated by company | |
| 24 Jun 2022 | Classified by FDA | +16 days |
| 6 Jul 2022 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Microbial contamination of non-sterile product: FDA laboratory analysis found product to contain elevated levels of yeast and mold as well as the presence of Bacillus cereus.
Product as listed by the FDA
Allergy Bee Gone for Kids Nasal Swab Remedy 0.33 FL OZ (10 mL) tubes, UPC Code 860002022116
Where it was distributed
Product was distributed via the internet to consumers, retailers and to distributors who may have further distributed the product.
Questions about this recall
Why was it recalled?
Microbial contamination of non-sterile product: FDA laboratory analysis found product to contain elevated levels of yeast and mold as well as the presence of Bacillus cereus.
Which lots are affected?
Lot #: 2006491, Exp. Date 08/24
Where was it sold?
Product was distributed via the internet to consumers, retailers and to distributors who may have further distributed the product.
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.