Advanced Accelerator Applications recalls PLUVICTO 1000MBq/mL vials with incorrect lot or expiration dates. Patients should check labels for correct lot numbers and expiration dates to avoid potential safety issues.
Labeling: Incorrect or Missing Lot and/or Exp Date: vials were labeled with the incorrect lot number and expiration date
Advanced Accelerator Applications is recalling PLUVICTO 1000MBq/mL vials that have incorrect lot numbers or expiration dates on the label. This could lead to improper use if the patient uses the vial after its expiration date or with the wrong lot number.
The vials were labeled with the wrong lot number and expiration date. This could lead to using the product after its expiration date or with the wrong lot number, which might affect treatment safety.
Patients using PLUVICTO 1000MBq/mL vials with incorrect lot numbers or expiration dates. Those who have the vial labeled with Lot # LPS230729B-16 (exp 8/3/2023) or LPS230804B-16 (exp 8/9/2023) are most at risk.
Check the label for lot number and expiration date. Affected vials have Lot # LPS230729B-16 (exp 8/3/2023) or LPS230804B-16 (exp 8/9/2023).
Verify the lot number and expiration date on the vial label to ensure they match the correct information.
The record does not specify the correct lot number.
The recall record does not specify the issue date.
Check the label for lot number LPS230729B-16 (exp 8/3/2023) or LPS230804B-16 (exp 8/9/2023).
We’ve drafted a message you can send Advanced Accelerator Applications to request your refund or repair — edit it as you like.
Subject: Recall D-1085-2023 — Advanced Accelerator Applications Advanced Accelerator Applications Hello, I own a Advanced Accelerator Applications that is covered by recall D-1085-2023 from Advanced Accelerator Applications. 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.
