Lohxa recalls SENNA Syrup (sennosides) 8.8 mg/5mL unit-dose cups due to microbial contamination. Affected units were manufactured for AvKARE with specific lot and expiration details.
“Lohxa SENNA Syrup Recall: Microbial Contamination Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/35420-lohxa-senna-syrup-recall-microbial-contamination-risk. Based on FDA recall #D-0377-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0377-2022%22&limit=1).
Lohxa, LLC recalled SENNA Syrup (sennosides) 8.8 mg/ 5 mL unit-dose cups due to microbial contamination risk, according to the FDA. The Food and Drug Administration announced the Class I recall on Dec. 21, 2021.
How to tell if you have it
Brand: Lohxa
Product: SENNA Syrup (sennosides) 8.8 mg/ 5 mL unit-dose cups, packaged in 24 cups per carton
NDC: 50262-731-24
Lot #: AM1115S
Exp. Date: 01/2023
Manufacturer for: AvKARE, TN 38478
The hazard
The product poses a risk of microbial contamination because it is a non-sterile product. The FDA classified the recall as Class I.
Context
GovInfoNow's records show Lohxa, LLC has two other recalls on record since March 25, 2019. On Oct. 28, 2020, Lohxa recalled Chlorhexidine Rinse due to microbial contamination risk involving Burkholderia lata bacteria. On March 25, 2019, Lohxa recalled Phenobarbital Oral Solution because the label contained an incorrect expiration date. Other recent recalls of similar products include Beekeeper's Naturals Saline Nasal Spray Recall (June 1, 2026), Victory Medical Center Pharmacy Glutathione Vials Recall (July 1, 2026), and Broadway Joe's Pain Cream Recall (Aug. 21, 2026).
How to tell if you have this one
Check for the product name 'SENNA Syrup (sennosides)', 8.8 mg/5mL unit-dose cups, packaged in 24 per carton. The lot number AM1115S and expiration date 01/2023 are specific identifiers for the recalled units.
Brand
Lohxa
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the lot number AM1115S and expiration date 01/2023 on the packaging to confirm if your product is affected.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Product was distributed to one wholesale who further distributed the product nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 11 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #D-0377-2022 (December 21, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0377-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.