Abbott Vascular recalls PLUS : 30 PRIORITY PACK Accessory Kit due to potential incorrect expiration entry for one lot. This may affect medical device safety during vascular procedures.
Incorrect expiration being entered for one lot.
Abbott Vascular is recalling the PLUS 30 PRIORITY PACK Accessory Kit because one lot may have incorrect expiration dates entered. This could lead to improper use during vascular procedures if the expiration date is not correctly identified.
Incorrect expiration dates entered for one lot could lead to using the kit after its expiration date. This might cause improper use during vascular procedures if the expiration date is not correctly identified.
Healthcare professionals using this kit during vascular procedures are likely affected. Those handling the specific lot number 60047593 are at higher risk.
Check for the lot number 60047593 on the PLUS 30 PRIORITY PACK Accessory Kit. This kit is used with interventional and diagnostic devices during vascular procedures.
Verify the expiration date on the kit's label to ensure it matches the correct date for lot 60047593.
Yes, this kit is recommended for use during vascular procedures with interventional and diagnostic devices.
Lot number 60047593 is affected by the incorrect expiration entry.
Check the lot number on the kit; if it is 60047593, it may be affected.
We’ve drafted a message you can send Abbott Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-0960-2019 — Abbott Vascular Abbott Vascular Hello, I own a Abbott Vascular that is covered by recall Z-0960-2019 from Abbott Vascular. 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.
