Failed Tablet/Capsule Specification; tablet breakage while pushing through the blister pack (dispenser) .
Failed Tablet/Capsule Specification; tablet breakage while pushing through the blister pack (dispenser) .
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Watson Laboratories Inc to request your refund or repair — edit it as you like.
Subject: Recall D-205-2013 — Watson Laboratories Inc Watson Laboratories Inc recalls ZARAH¿ Drospirenone/ Ethinyl Estradiol Table Hello, I own a Watson Laboratories Inc recalls ZARAH¿ Drospirenone/ Ethinyl Estradiol Tablets, 3.0 mg/0.03 mg, Rx only, 3 tablet dispensers, 28 tablets each, Manuf. that is covered by recall D-205-2013 from Watson Laboratories Inc. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
