FDA DrugsClass I
ClearLife Allergy Nasal Spray, Extra Strength, 0.68 fl. oz. (20 mL) bottles, Dis...
Published: January 14, 2026Recall ID: D-0289-2026Category: drugsCountry: US
Reason for Recall / Hazard
Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
Product Description & Identification
ClearLife Allergy Nasal Spray, Extra Strength, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM 87123, NDC 62795-4006-9, UPC 787647101887
Additional Source Details
| Field | Value |
|---|---|
| City | Albuquerque |
| State | NM |
| Openfda › Nui › 1 | N0000185371 |
| Openfda › Nui › 2 | N0000175629 |
| Openfda › Nui › 3 | N0000184306 |
| Openfda › Nui › 4 | M0000728 |
| Openfda › Nui › 5 | M0006342 |
| Openfda › Nui › 6 | M0022575 |
| Openfda › Upc | 787647101887 |
| Openfda › Unii › 1 | 9W34L2CQ9A |
| Openfda › Unii › 2 | C9642I91WL |
| Openfda › Unii › 3 | 93PH5Q8M7E |
| Openfda › Unii › 4 | 3POA0Q644U |
| Openfda › Unii › 5 | C4MO6809HU |
| Openfda › Unii › 6 | 492225Q21H |
| Openfda › Unii › 7 | 6NAF1689IO |
| Openfda › Unii › 8 | 70FD1KFU70 |
| Openfda › Route | NASAL |
| Openfda › Spl id | c5d30dbc-f317-4ff1-86b6-8d57bfb0da75 |
| Openfda › Brand name | CLEARLIFE EXTRA STRENGTH |
| Openfda › Spl set id | 09fbebf9-3d8b-479c-80f3-37f07cb699d6 |
| Openfda › Package ndc › 1 | 62795-4006-9 |
| Openfda › Package ndc › 2 | 7876471018 |
| Openfda › Product ndc | 62795-4006 |
| Openfda › Generic name | ONION, GALPHIMIA GLAUCA FLOWERING TOP, HISTAMINE DIHYDROCHLORIDE, LUFFA OPERCULATA FRUIT, SULFUR, AMBROSIA ARTEMISIIFOLIA WHOLE, EUPHRASIA STRICTA AND SCHOENOCAULON OFFICINALE SEED |
| Openfda › Product type | HUMAN OTC DRUG |
| Openfda › Pharm class cs › 1 | Allergens [CS] |
| Openfda › Pharm class cs › 2 | Dietary Proteins [CS] |
| Openfda › Pharm class cs › 3 | Vegetable Proteins [CS] |
| Openfda › Pharm class pe › 1 | Increased Histamine Release [PE] |
| Openfda › Pharm class pe › 2 | Cell-mediated Immunity [PE] |
| Openfda › Substance name › 1 | AMBROSIA ARTEMISIIFOLIA WHOLE |
| Openfda › Substance name › 2 | EUPHRASIA STRICTA |
| Openfda › Substance name › 3 | GALPHIMIA GLAUCA FLOWERING TOP |
| Openfda › Substance name › 4 | HISTAMINE DIHYDROCHLORIDE |
| Openfda › Substance name › 5 | LUFFA OPERCULATA FRUIT |
| Openfda › Substance name › 6 | ONION |
| Openfda › Substance name › 7 | SCHOENOCAULON OFFICINALE SEED |
| Openfda › Substance name › 8 | SULFUR |
| Openfda › Pharm class epc | Non-Standardized Food Allergenic Extract [EPC] |
| Openfda › Manufacturer name | MediNatura Inc. |
| Openfda › Is original packager | true |
| Event id | 98095 |
| Address 1 | 10421 Research Rd Se |
| Code info | All lots within expiry. |
| Postal code | 87123-3423 |
| Report date | 20260114 |
| Product type | Drugs |
| Reason for recall | Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20251212 |
| Initial firm notification | Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit |
| Center classification date | 20260115 |
Overview
- Recalling FirmMedinatura New Mexico, inc.
- StatusOngoing
- Risk LevelClass I
- DistributionNationwide in the US