Lower riskDrug recall · FDA · Published March 25, 2019
Lohxa Bismuth Subsalicylate Oral Suspension: Incorrect Exp Date on Label
Lohxa recalls Bismuth Subsalicylate Oral Suspension 262mg/15mL unit dose cups due to incorrect expiration date on labels. Consumers should check labels for lot number M030042P and expiration date 01/2020.
“Lohxa Bismuth Subsalicylate Oral Suspension: Incorrect Exp Date on Label.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/39069-lohxa-bismuth-subsalicylate-oral-suspension-incorrect-exp-date-on-label. Based on FDA recall #D-1130-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1130-2019%22&limit=1).
Lohxa LLC voluntarily recalled Bismuth Subsalicylate Oral Suspension due to an incorrect expiration date on the label, according to the FDA. The Food and Drug Administration announced the Class II recall on March 25, 2019.
How to tell if you have it
Brand: Lohxa
Product: Bismuth Subsalicylate Oral Suspension 262mg/15mL, unit dose cups, OTC, Rpkg. By.: Lohxa Worcester, MA
NDC: 70166-059-01
Lot#: M030042P
Exp. 01/2020
Distribution: MA, NY and WY
The hazard
The hazard is labeling error because the label contains an incorrect expiration date.
Context
GovInfoNow's records show Lohxa, LLC has two other recalls on record since October 28, 2020. Other recent recalls of similar products include Premier Dental Products: Incorrect Expiration Date on Ferric Subsulfate Solution (April 14, 2026), OurPharma Fentanyl Injection Recall: IV Bag Expiry Discrepancy (September 3, 2026), and Safecor Health Fluphenazine Elixir Recall: Failed Stability Specifications (August 13, 2026).
How to tell if you have this one
Check the label for lot number M030042P and expiration date 01/2020. The product is a Bismuth Subsalicylate Oral Suspension 262mg/15mL unit dose cup sold by Lohxa.
Brand
Lohxa
Category
Drug
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
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-1130-2019 (March 25, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1130-2019 to see it in context.
Plain-language summary written by qwen3:4b on October 5, 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.