Mckesson recalls Medefil Normal Saline IV Flush Syringes (MIS-1130) produced between June 2021 and August 2021 due to potential temperature excursions affecting product effectiveness. Consumers should check their purchase dates and model numbers.
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 is recalling Medefil Normal Saline IV Flush Syringes (MIS-1130) that were produced between June 1, 2021 and September 30, 2021. These syringes may have been affected by temperature excursions during shipping, which could impact their effectiveness for medical use.
The syringes were potentially exposed to higher temperatures during shipping from June 2021 to August 2021, which could have reduced their effectiveness as a medical product. This is a quality issue rather than a safety hazard that could cause injury.
Healthcare facilities and medical professionals who used these syringes between June 2021 and August 2021 are most at risk. The recall affects specific batches produced during that time period.
Check for the model number MIS-1130 on the syringe packaging. The product was sold between June 1, 2021 and September 30, 2021. Look for GTIN numbers listed in the recall notice.
Verify the production date of your syringes to ensure they were manufactured between June 1, 2021 and September 30, 2021.
The syringes may have been affected by temperature excursions during shipping from June 2021 to August 2021, which could impact their effectiveness as a medical product.
The affected model number is MIS-1130. The product was sold with specific GTIN numbers listed in the recall notice.
No, the recall is for potential quality issues, not a safety hazard. The product remains safe for use but may not be as effective as intended.
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-1619-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall Z-1619-2022 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.
