Recall events
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Event 98037
Event summary
Timeline bucket November 20, 2025
Product types Food
Classifications Class II
Statuses Ongoing
Recalling firm wording A New Life Herbs, LLC
Dossier provenance
Source snapshots represented here
openFDA Food Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Device root-cause evidence is not applicable to this event.
No grouped product has the official product type device; this is not an unavailable-enrichment finding.
Complete imported group
Every recalled product in this event
9 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
food · product 1 of 9
Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to stop viral replication, expectorant properties, Contains: Forsethia blossoms, Sumac berries, Pine needles; packaged in a 2 oz. glass dropper bottle, UPC 283162814429
H-0340-2026
Recall number H-0340-2026
Initiated November 20, 2025
Classification Class II
Status Ongoing
Quantity 116 bottles
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
misbranded
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Code information T801AV EXP 9/30 T686AV EXP 12/29 T636AV EXP 9/29 T564AV EXP 9/28
Distribution pattern AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[549]
FDA event record
· Exact recall-number query on openFDA
food · product 2 of 9
Baby Allergy Herbal Supplement, Contains: Echinacea Purpurea, Oregon Grape Root, Dandelion & Burdock Root, Fenugreek, Ginger Root in vegetable glycerin; packaged in a 2 oz. glass dropper bottle, UPC 249953949282
H-0341-2026
Recall number H-0341-2026
Initiated November 20, 2025
Classification Class II
Status Ongoing
Quantity 23 bottles
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
misbranded
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Code information E166SA EXP 4/28
Distribution pattern AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[539]
FDA event record
· Exact recall-number query on openFDA
food · product 3 of 9
Baby Soothe Herbal Supplement, Promotes rest, helps ease colic, upset stomach, and teething discomfort, Contains: Catnip, Chamomile, Vegetable Glycerin, water; packaged in a 2 oz. glass dropper bottle
H-0342-2026
Recall number H-0342-2026
Initiated November 20, 2025
Classification Class II
Status Ongoing
Quantity 49 bottles
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
misbranded
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Code information E164BS EXP 1/27 E128BS EXP 7/26
Distribution pattern AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[535]
FDA event record
· Exact recall-number query on openFDA
food · product 4 of 9
Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, Extracted from Frankincense with powerful anti-inflammatory properties, useful for pain & inflammation; packaged in a 2 oz. glass dropper bottle, UPC 284260392420
H-0343-2026
Recall number H-0343-2026
Initiated November 20, 2025
Classification Class II
Status Ongoing
Quantity 278 bottles
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
misbranded
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Code information T848B EXP 11/30 T836B EXP 10/30 T808B EXP 9/30 T771B EXP 7/30 T723B EXP 3/30 T696B EXP 1/29 T655B EXP 10/29 T594B EXP 4/29 T536B EXP 10/28
Distribution pattern AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[504]
FDA event record
· Exact recall-number query on openFDA
food · product 5 of 9
Chaga Mushroom Herbal Supplement, 1:5 Alcohol Double Extract, Supports a healthy immune system with anti-cancer properties; packaged in a 2 oz. glass dropper bottle, UPC 284588087831
H-0344-2026
Recall number H-0344-2026
Initiated November 20, 2025
Classification Class II
Status Ongoing
Quantity 144 bottles
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
misbranded
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Code information T720CH EXP 3/30 T656CH EXP 10/29 T618CH EXP 7/29 T568CH EXP 1/29 T532CH EXP 10/28
Distribution pattern AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[547]
FDA event record
· Exact recall-number query on openFDA
food · product 6 of 9
Ear Drops Herbal Supplement, Mullein flower alcohol tincture 1:5, Pain relieving and antibiotic properties, packaged in a 0.5 oz. plastic dropper bottle
H-0345-2026
Recall number H-0345-2026
Initiated November 20, 2025
Classification Class II
Status Ongoing
Quantity 22 bottles
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
misbranded
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Code information T553MF EXP 12/28
Distribution pattern AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[502]
FDA event record
· Exact recall-number query on openFDA
food · product 7 of 9
Organic Ginger Root Herbal Supplement, Natural anti-inflammatory properties, supports gut, increases circulation, 50 capsules/560 mg, packaged in a plastic bag
H-0346-2026
Recall number H-0346-2026
Initiated November 20, 2025
Classification Class II
Status Ongoing
Quantity 48 bags
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
misbranded
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Code information C132GR EXP 7/27 C131GR EXP 6/27 C121GR EXP 2/27 C115GR EXP 12/26 C108GR EXP 1/26 C93GR EXP 7/25
Distribution pattern AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[514]
FDA event record
· Exact recall-number query on openFDA
food · product 8 of 9
Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties, Wood Betony & White Willow in vegetable glycerin, packaged in a 4.5 oz. glass bottle or 9 oz. glass bottle, UPC 231946534537
H-0347-2026
Recall number H-0347-2026
Initiated November 20, 2025
Classification Class II
Status Ongoing
Quantity 275 bottles
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
misbranded
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Code information E170PA EXP 7/28 E174PA EXP 9/28 E161PA EXP 12/27 E146PA EXP 12/26 E123PA EXP 7/26 E110PA EXP 10/25 E93PA EXP 2/25
Distribution pattern AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[478]
FDA event record
· Exact recall-number query on openFDA
food · product 9 of 9
Sinus Cap Herbal Supplement, Herbs containing antibiotic, drying, expectorant, and emollient properties, Fenugreek, Thyme, Oregon Grape Root, & Bentonite Clay, 50 capsules/510 mg; packaged in a plastic bag
H-0348-2026
Recall number H-0348-2026
Initiated November 20, 2025
Classification Class II
Status Ongoing
Quantity 38 bags
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
misbranded
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Code information C136SC EXP 10/27 C128SC EXP 5/27 C110SC EXP 9/26 C109SC EXP 4/26 C102SC EXP 10/25
Distribution pattern AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[508]
FDA event record
· Exact recall-number query on openFDA
