Teva Pharmaceuticals recalls Fentanyl Buccal Tablets (200mcg) due to missing package inserts. This could lead to incorrect use. Consumers should contact the manufacturer for details.
Labeling: Incorrect or Missing Package Insert
Teva Pharmaceuticals is recalling Fentanyl Buccal Tablets (200mcg) because the package insert may be missing or incorrect. This could lead to improper use of the medication, which is dangerous for patients.
The package insert, which contains critical instructions for safe use, may be missing or incorrect. Without this, patients might not understand how to use the medication properly, increasing the risk of misuse or adverse effects.
Patients prescribed Fentanyl Buccal Tablets by a doctor. Those using the medication without proper instructions are at higher risk.
Check for the product name 'Fentanyl Buccal Tablets CII, 200mcg' in cartons of 28 tablets (4 tablets x 7 cards). The lot numbers 100020528 (expiring 09/2024) and 100026699 (expiring 11/2024) are affected.
Ensure the package insert is present and correct before using the medication.
The recall is due to missing or incorrect package inserts, which could lead to improper use. The official notice does not specify if the product is dangerous without the insert.
Check for the product name 'Fentanyl Buccal Tablets CII, 200mcg' in cartons of 28 tablets (4 tablets x 7 cards) with lot numbers 100020528 (expiring 09/2024) or 100026699 (expiring 11/2024).
The recall does not specify a remedy. Contact Teva Pharmaceuticals for further instructions.
We’ve drafted a message you can send Teva Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0767-2023 — Teva Pharmaceuticals Teva Pharmaceuticals Hello, I own a Teva Pharmaceuticals that is covered by recall D-0767-2023 from Teva Pharmaceuticals. 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.
