Teva Recalls Zebeta 10mg Tablets Due to Dissolution Failure
Teva Pharmaceuticals recalls 889 bottles of Zebeta 10mg tablets (Lot 34019710A) due to failed dissolution specifications. Check your medication bottle.
Use caution until it’s fixed
Failed Dissolution Specifications: OOS result during stability testing
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What happened, in plain English
Teva Pharmaceuticals USA has recalled a specific lot of Zebeta (bisoprolol fumarate) 10mg tablets because they failed dissolution specifications during stability testing. The affected product is a 30-count, prescription-only bottle distributed nationwide. This recall affects Lot #34019710A with an expiration date of May 2017. Read more at govinfonow.com/recall/44710-teva-pharmaceuticals-usa-recalls-zebeta-bisoprolol-fumarate-tablets-10mg-30.
Source Summary by GovInfoNow · govinfonow.com/recall/44710-teva-pharmaceuticals-usa-recalls-zebeta-bisoprolol-fumarate-tablets-10mg-30 · Updated October 12, 2026 · FDA enforcement record: FDA #D-1112-2015
Cite this page
“Teva Recalls Zebeta 10mg Tablets Due to Dissolution Failure.” GovInfoNow, updated October 12, 2026. https://govinfonow.com/recall/44710-teva-pharmaceuticals-usa-recalls-zebeta-bisoprolol-fumarate-tablets-10mg-30. Based on FDA recall #D-1112-2015 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1112-2015%22&limit=1).
Why it’s dangerous
The tablets failed dissolution specifications, meaning they may not break down or release the active ingredient as intended in the body. This could result in the medication not working effectively to treat the patient's condition.
Who’s affected
Individuals who have been prescribed Zebeta (bisoprolol fumarate) 10mg tablets and possess the specific recalled lot. Patients relying on this medication for heart conditions may be at risk if the drug does not dissolve properly.
How to tell if you have this one
Check your bottle for NDC 51285-061-01 and Lot #34019710A. The product is a 10mg, 30-count bottle of Zebeta tablets manufactured by Duramed Pharmaceuticals, Inc. for Teva Pharmaceuticals.
- Brand
Teva- Category
Drug
What to do — step by step
Check your medication
Verify if your Zebeta bottle matches NDC 51285-061-01 and Lot #34019710A with an expiration date of May 2017.
Contact your pharmacist
If you have the recalled lot, contact your pharmacy or healthcare provider to discuss replacing the medication.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 18 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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-1112-2015 (May 11, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1112-2015 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 12, 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.