MEDLINE SYR 10ML L/L CONTROL syringes (model 91881) may not be safe for medical use due to incorrect size configurations. Affected units include specific lot codes from June 2023. Consumers should check their syringes and contact MEDLINE for details.
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
MEDLINE is recalling SYR 10ML L/L CONTROL syringes (model 91881) because they may not be safe for medical use. These syringes could cause harm if used incorrectly due to mismatched sizes with medical devices.
The syringes have sizes and configurations that do not match the medical devices cleared by the manufacturer. This mismatch could lead to improper use or ineffective medical treatments if the syringes are used with devices they were not designed for.
People who own or use MEDLINE SYR 10ML L/L CONTROL syringes (model 91881) with specific lot codes are affected. Healthcare professionals and patients using these syringes for medical purposes are most at risk.
Check for the model number 91881 on the syringe packaging. Affected units include specific lot codes listed in the recall notice, such as LOT: 63721010001 through LOT: 63723110003.
Look for the model number 91881 on the syringe packaging or label.
Reach out to MEDLINE directly for assistance with the recall and to confirm if your syringes are affected.
The recall states that these syringes may not be safe for medical use due to incorrect size configurations. They should not be used without confirming they are safe.
Affected lot codes include specific numbers listed in the recall, such as LOT: 63721010001 through LOT: 63723110003.
The recall does not specify a replacement process. Contact MEDLINE directly for details on what to do with affected syringes.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2099-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2099-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
