B. Braun recalls 1000 mL EVA Gravity Mixing Containers with model 2112363 made between June 1 and September 30, 2021 due to potential temperature issues affecting product effectiveness.
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.
B. Braun is recalling 1000 mL EVA Gravity Mixing Containers with model number 2112363 that were manufactured between June 1 and September 30, 2021. These containers may have been affected by temperature excursions during shipping, which could impact their effectiveness.
The containers were exposed to higher temperatures during shipping from June 2021 to August 2021, which could have reduced their effectiveness. This risk is specific to the temperature conditions during transit and does not involve immediate safety hazards.
Healthcare facilities that received these containers between June 1 and September 30, 2021 are likely affected. Staff using these containers for medical purposes may be at risk if the product's effectiveness is compromised.
Check for the model number 2112363 on the container. These containers were sold between June 1 and September 30, 2021, and have specific GTIN numbers.
Verify the model number and date range to confirm if your container is affected.
The containers may have been affected by temperature excursions during shipping from June 2021 to August 2021, which could impact product effectiveness.
The official recall notice does not specify a remedy or action steps for affected products.
The recall indicates a potential issue with product effectiveness due to temperature exposure, but no immediate safety hazards are mentioned.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-1592-2022 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-1592-2022 from B. Braun. 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.
