Medline convenience kits with specific model numbers and pack numbers were recalled due to plastic syringes that may leak or break, posing a risk to patient health. Affected kits include GER ARTH BASIN PK RFID-LF and others listed in the recall notice.
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
Medline convenience kits containing plastic syringes that may leak or break have been recalled. This risk could affect patient health, so users should stop using these kits immediately.
The plastic syringes in these kits have been identified by the FDA as having leaks, breakage, and other quality issues. These problems could lead to contamination or injury to patients during medical procedures.
Healthcare professionals and patients who use Medline convenience kits with the listed model numbers and pack numbers are most at risk. These kits are used in medical settings for procedures like surgeries and treatments.
Check for kits labeled with model names like GER ARTH BASIN PK RFID-LF, PEDIATRIC MAJOR BASIN, or other specific pack numbers listed in the recall notice. The pack numbers are detailed in the record.
Immediately stop using any Medline convenience kits with the specific model numbers and pack numbers listed in the recall notice.
The affected kits include GER ARTH BASIN PK RFID-LF, PEDIATRIC MAJOR BASIN, and other specific model names with pack numbers listed in the recall notice.
Check the model name and pack number on your kit. The affected kits are listed in the recall notice with specific pack numbers and model names.
The recall notice does not mention any replacements or remedies.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3018-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3018-2024 from Medline. 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.
