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Unrated Drug recall · FDA · Published April 29, 2015

Ortho-Cept

Subpotent Drug

🇺🇸 FDA recall #D-1063-2015DrugJanssen Pharmaceuticals, Inc. ›
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Recalling firmJanssen Pharmaceuticals, Inc.1125 Trenton-Harbourton Rd · Titusville, NJ 08560-1503
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Source Page by GovInfoNow · govinfonow.com/recall/44721-janssen-pharmaceuticals-inc-recalls-ortho-cept-0-15-mg-desogestrel · Recall date April 29, 2015 · FDA enforcement record: FDA #D-1063-2015

Cite this page

“Ortho-Cept.” GovInfoNow, recall dated April 29, 2015. https://govinfonow.com/recall/44721-janssen-pharmaceuticals-inc-recalls-ortho-cept-0-15-mg-desogestrel. Based on FDA recall #D-1063-2015 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1063-2015%22&limit=1).

How to tell if you have this one

  • Brand
    Janssen Pharmaceuticals, Inc.
  • Category
    Drug

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

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 and Canada” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 3.2 years after the firm started it.

1. Firm started the recall: Apr 29, 201512. FDA classified it Class II: May 11, 201523. Published in FDA’s Enforcement Report: May 20, 201534. FDA terminated the recall: Jul 13, 2018420152018
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. 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-1063-2015 (April 29, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1063-2015 to see it in context.
  • 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