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Lower risk Drug recall · FDA · Published February 7, 2022

Rising Pharmaceuticals Methylphenidate Tablets Recall: Size Variation Risk

Rising Pharmaceuticals recalls 2.5 mg chewable methylphenidate tablets due to size variation in some tablets. This may affect safety and requires verification of product details.

🇺🇸 FDA recall #D-0573-2022DrugRising Pharmaceuticals ›
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Recalling firmRISING PHARMACEUTICALS2 Tower Center Blvd · East Brunswick, NJ 08816-1100
✎ GovInfoNow plain-language explainer

Rising Pharmaceuticals is recalling 2.5 mg chewable methylphenidate tablets because some tablets in the sealed bottle are twice the size of others. This variation could lead to inconsistent dosing and potential safety risks for users. Read more at govinfonow.com/recall/35234-rising-pharmaceuticals-methylphenidate-tablets-recall-size-variation-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/35234-rising-pharmaceuticals-methylphenidate-tablets-recall-size-variation-risk · Updated August 18, 2026 · FDA enforcement record: FDA #D-0573-2022

Cite this page

“Rising Pharmaceuticals Methylphenidate Tablets Recall: Size Variation Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/35234-rising-pharmaceuticals-methylphenidate-tablets-recall-size-variation-risk. Based on FDA recall #D-0573-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0573-2022%22&limit=1).

Rising Pharmaceuticals voluntarily recalled Methylphenidate Hydrochloride Chewable Tablets, 2.5 mg, 100-count bottles due to failed tablet specifications, according to the FDA on Feb. 7, 2022. The recall was initiated after a complaint reported a tablet twice the normal size.

How to tell if you have it

  • Brand: Rising Pharmaceuticals
  • Product: Methylphenidate Hydrochloride Chewable Tablets, 2.5 mg, 100-count bottle
  • NDC: 64980-221-01
  • Lot code: 25910009
  • Expiration date: 01/2023
  • Quantity: 2,220 bottles
  • Distribution: Nationwide in the USA

The hazard

The recall addresses failed tablet specifications where a tablet was found to be twice larger than the remaining tablets in the sealed bottle. This complaint marks the second instance of this specific issue.

Context

GovInfoNow's records show Rising Pharmaceuticals has two other recalls on record since Sept. 2, 2021, including a Feb. 15, 2023 recall for Warfarin Tablets due to impurities risk and a Sept. 2, 2021 recall for Meclizine Tablets involving incorrect instructions. Other recent recalls of similar products include Major Pharmaceuticals Levothyroxine Tablets Recall (July 13, 2026), Alvogen Thyro-Tabs 150mcg Tablets Recall (Dec. 31, 2025), and Winder Morphine Sulfate Oral Solution Recall (Nov. 26, 2025).

How to tell if you have this one

Check for the product name 'Methylphenidate Hydrochloride Chewable Tablets, 2.5 mg, 100-count bottle' with the lot number 25910009 and expiration date 01/2023. The product is manufactured by Rising Pharmaceuticals in Saddle Brook, NJ.

  • Brand
    Rising Pharmaceuticals
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify the product's lot number (25910009) and expiration date (01/2023) to confirm if it is recalled.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “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 published this recall 23 days after the firm started it.

1. Firm started the recall: Feb 7, 202212. FDA classified it Class II: Feb 22, 202223. Published in FDA’s Enforcement Report: Mar 2, 202232022
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

Is there a risk of serious injury from this product?

The recall is due to size variation, which could affect dosing consistency but does not indicate a risk of serious injury in normal use.

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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-0573-2022 (February 7, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0573-2022 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA