📍Recalling firmAmerican Health Packaging2550 John Glenn Ave, Suite A · Columbus, OH 43217-1188
✎ GovInfoNow plain-language explainer
American Health Packaging is recalling Methylprednisolone Tablets, USP, 4 mg, packaged in 100-unit dose blisters. The recall was initiated because stability testing at the 6-month time point indicated the tablets may be subpotent. This means the medication might not contain the full amount of active ingredient required for effective treatment. Read more at govinfonow.com/recall/45671-american-health-packaging-recalls-methylprednisolone-tablets-usp-4-mg-100.
“Recall: American Health Methylprednisolone 4mg Tablets Due to Subpotency.” GovInfoNow, updated October 12, 2026. https://govinfonow.com/recall/45671-american-health-packaging-recalls-methylprednisolone-tablets-usp-4-mg-100. Based on FDA recall #D-0043-2015 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0043-2015%22&limit=1).
American Health Packaging recalled Methylprednisolone Tablets, USP, 4 mg due to subpotency issues, the FDA said on Oct. 10, 2014. The Class III recall involved 2,005 cartons distributed nationwide.
How to tell if you have it
Brand: American Health Packaging
Product: Methylprednisolone Tablets 4 mg
NDC 68084-149-01 (Carton)
NDC 68084-149-11 (Individual Dose)
Lot #: 134124 and 140364
Expiration Date: 05/2015
The hazard
The recall was initiated because the Methylprednisolone Tablets were found to be subpotent at the six-month stability time point. The FDA classified this as a Class III recall.
Context
GovInfoNow's records show American Health Packaging has 41 other recalls on record since July 23, 2012. Other recent recalls of similar products include American Health Packaging Buprenorphine Tablets Recall (Aug. 19, 2026), American Health Packaging Nitrofurantoin Capsules Recall (May 3, 2022), and American Health Packaging Recalls Cyanocobalamin Injection Due to Subpotent Drug (April 12, 2022). Other recent recalls of similar products include Unichem busPIRone 5mg Tablets Recall (April 13, 2026), Major Pharmaceuticals Levothyroxine Tablets Recall (July 13, 2026), and Specialty Process Labs Thyroid Product Recall (Jan. 16, 2026).
How to tell if you have this one
Check your medication packaging for the following details: Product is Methylprednisolone Tablets, USP, 4 mg, in 100-unit dose blisters. Look for NDC numbers 68084-149-01 (Carton) and 68084-149-11 (Individual Dose). Verify the AHP Lot numbers are 134124 or 140364, both with an expiration date of 05/2015.
Brand
American Health Packaging
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check your medication details
Verify if your Methylprednisolone tablets match the recalled NDC numbers (68084-149-01 or 68084-149-11) and lot numbers (134124 or 140364).
Consult your healthcare provider
Contact your doctor or pharmacist to discuss whether you should replace the recalled medication with a different lot or manufacturer.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
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 8 months after the firm started it.
1Firm started the recall
2FDA classified it Class III
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-0043-2015 (October 10, 2014) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0043-2015 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.