Quick Facts at a Glance
- Recall Date
- January 29, 2026
- Hazard Level
- HIGH
- Brand
- Metoprolol Succinate
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Metoprolol Succinate
- Product type
- Metoprolol Succinate Extended-Release Tablets 25 mg
- Model numbers
- 0715J251, 0716J251, 0717J251, 0715J252, 0716J252, 0717J252
- UPC codes
- 45963-676, 45963-709, 45963-677, 45963-678, 45963-709-11, 45963-709-96, 45963-676-11, 45963-676-96 +3 more
- Sizes
- 100-tablet bottle, 1000-tablet bottle
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
January 29, 2026
Reported by FDA DRUG
March 11, 2026
RecallRadar source check
March 18, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Failed Dissolution Specifications
What You Should Do
Consumers and healthcare providers should stop using this product immediately. Contact Teva Pharmaceuticals USA, Inc or your healthcare provider for guidance. Notification method: Letter
About This Product
Metoprolol succinate extended-release tablets are a generic beta-blocker used to treat high blood pressure, chest pain, and certain heart conditions. They are available in 25 mg extended-release tablets in 100-tablet and 1000-tablet bottles.
Why This Is Dangerous
Dissolution specification failure means the tablet may not release the drug consistently, potentially leading to underdosing and reduced treatment effectiveness.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Patients relying on consistent dosing may experience unmanaged blood pressure or heart rate. There are no reported injuries or deaths in this recall.
Practical Guidance
How to identify if yours is affected
- Check NDCs 45963-709-11 and 45963-709-96 on your bottle
Where to find product info
Bottle label shows NDC and lot number; official recall page listed in article.
What timeline to expect
4-6 weeks for recall processing is typical; actual processing times vary by manufacturer and pharmacy.
If the manufacturer is unresponsive
- Document all contact attempts with Teva and your healthcare provider
- File a complaint with the FDA if the company is unresponsive
- Consult your pharmacist for guidance on alternatives
How to prevent similar issues
- Regularly check recalls for prescription medications on FDA and manufacturer sites
- Always verify NDC and lot numbers when receiving medications
- Discuss any recalls with your healthcare provider before continuing treatment
Documentation advice
Keep the recall notice, bottle labels showing NDC and lot numbers, and all correspondence with Teva or your provider.
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Product Details
Product: Metoprolol Succinate Extended-Release Tablets, 25 mg. NDCs: 45963-709-11 (100-tablet bottles) and 45963-709-96 (1000-tablet bottles). Quantity recalled: 18,780 bottles. Manufacturer: Teva Pharmaceuticals USA, Parsippany, NJ 07054. Sold nationwide as Rx-only.
Key Facts
- 18,780 bottles recalled nationwide
- Remedy: Stop use and contact Teva or your healthcare provider
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
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