MEDLINE 10ml blue syringes (model 91832) may not meet FDA safety standards due to incorrect size configurations. Affected units include specific lot codes. 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 10ml blue syringes (model 91832) are being recalled because they don't match the approved design for medical use. This could lead to improper dosing if used with certain medical devices.
The syringes have sizes and configurations that don't match the medical devices cleared by the FDA. This could cause incorrect dosing if used with devices that require specific syringe types.
Medical professionals and patients using these syringes for injections. Those with specific medical devices that require precise syringe sizes are at higher risk.
Check for the model number 91832 on the syringe. Look for lot codes: 63721010001 through 63723120002. These syringes are non-sterile and without needles for single use.
Look for the model number 91832 on the syringe.
Reach out to MEDLINE for specific instructions on how to handle affected units.
The recall indicates they may not meet FDA safety standards for medical use due to incorrect size configurations. They are not recommended for use with devices that require specific syringe types.
Check the model number and lot codes. Contact MEDLINE for specific instructions on handling affected units.
Look for the model number 91832 and lot codes from 63721010001 to 63723120002 on the syringe.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2064-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2064-2024 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.
