Baxter recalls yellow self-righting Luer slip syringe tip caps (REF H93866100) due to mislabeling. Check lot numbers 60268365, 60268609, 60268610 with expiration 10/31/2023 for affected units.
Product is mislabeled as self-righting Luer slip tip caps, yellow.
Baxter is recalling yellow self-righting Luer slip syringe tip caps that are mislabeled as self-righting. This mislabeling means users might not know they have the wrong product, which could lead to incorrect use in medical settings.
The product is mislabeled as self-righting Luer slip tip caps, yellow. This means the actual product may not function as intended for medical use, potentially causing incorrect application or handling errors in clinical settings.
Healthcare professionals and patients using Baxter DISCPAC syringe tip caps with the specific lot numbers and expiration date mentioned. Those most at risk are individuals handling medical equipment without verifying the product label.
Check for the product name 'Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow, REF H93866100' with lot numbers 60268365, 60268609, 60268610 and expiration date 10/31/2023.
Look for lot numbers 60268365, 60268609, 60268610 and expiration date 10/31/2023 on the syringe tip caps.
The product is mislabeled as self-righting Luer slip tip caps, yellow. Using them without verifying the label could lead to incorrect application in medical settings.
The recall does not specify a remedy, so check the product label for lot numbers and expiration date to determine if you have affected units.
Look for the product name 'Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow, REF H93866100' with lot numbers 60268365, 60268609, 60268610 and expiration date 10/31/2023.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-0948-2022 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0948-2022 from Baxter. 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.
