Cardinal Health recalls specific Jackson-Pratt 3-Spring Reservoir kits shipped without proper sterilization. These kits may cause infection if used. Affected units have unique lot numbers and were sold in 2019-2020.
Cardinal Health is issuing a lot number specific voluntary removal of Jackson-Pratt 3-Spring Reservoir kits due to specific products being shipped to users before undergoing sterilization.
Cardinal Health is recalling certain Jackson-Pratt 3-Spring Reservoir kits that were shipped to users before undergoing sterilization. Using these kits without proper sterilization could lead to infection risks.
The kits were shipped to users before completing sterilization. This means they could be contaminated and cause infections if used in medical procedures.
Medical professionals and patients using the recalled kits for drainage procedures. Those who received the kits with lot numbers listed above are most at risk.
Check the lot numbers on the kit: 231251D2, 231252D2, 231253D2, 231254D2, 231255D2, 231256D2, 231151D2, 231152D2, 231153D2, 210751D2, 210752D2, 210753D2, 210754D2, 210755D2. These kits were sold between 2019 and 2020.
Look for the specific lot numbers listed in the recall notice to identify affected units.
The kits were shipped to users before undergoing sterilization, which could lead to contamination and infection risks.
The recall notice does not specify a remedy, so contact Cardinal Health directly for guidance.
Using unsterilized kits could lead to infection risks, but the recall does not indicate immediate danger for all users.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-1736-2024 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-1736-2024 from Cardinal Health. 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.
