Mckesson Medical-Surgical recalls Perifix LOR Syringe model 332152 due to potential temperature excursions affecting product effectiveness. All units shipped between June 2021 and August 2021 are affected.
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.
Mckesson Medical-Surgical is recalling Perifix LOR Syringes with model number 332152 because they may have been exposed to temperatures that could reduce their effectiveness. This recall affects syringes shipped between June 1, 2021, and August 30, 2021.
The syringes were shipped during a period when facility temperatures may have fluctuated, potentially reducing their effectiveness. This could lead to improper medication delivery if the syringe does not function as intended.
Healthcare facilities that received Perifix LOR Syringes with model number 332152 between June 1, 2021, and August 30, 2021 are likely affected. Medical staff using these syringes for procedures may be at risk if the product's effectiveness is compromised.
Check for the model number 332152 on the syringe packaging. The recall covers all units shipped between June 1, 2021, and August 30, 2021.
Verify the model number on the syringe packaging to confirm if it matches 332152.
The recall is due to potential temperature excursions during shipping from June 2021 to August 2021, which may have impacted the syringe's effectiveness.
Model number 332152 (Perifix LOR Syringe Perifix 8 mL Pouch Luer Lock Tip Without Safety).
All units shipped between June 1, 2021, and August 30, 2021 are affected.
We’ve drafted a message you can send Mckesson Medical-Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-1591-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall Z-1591-2022 from Mckesson Medical-Surgical. 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.
