MEDLINE recalls SYR 20ML L/L BLUE SALINE syringes (model 91845) due to piston size mismatch with cleared devices. Non-sterile single-use syringes without needles.
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
MEDLINE is recalling SYR 20ML L/L BLUE SALINE syringes (model 91845) because their piston size doesn't match devices cleared by the manufacturer. This could lead to improper use if the syringe is used with devices it wasn't designed for.
The syringes have piston sizes and configurations that don't match the devices cleared by the manufacturer. This mismatch could cause improper use if the syringe is used with devices it wasn't designed for, potentially leading to incorrect dosing or device damage.
Users of non-sterile syringes without needles for single use. Most at risk are healthcare professionals or individuals administering injections.
Check for model number 91845 on the syringe. Look for lot codes: 63721060001, 63721070001, 63722020002, 63722030001, 63722040004, 63722090002, 63722100003, 63723020001, 63723060001, 63723090002.
Look for model number 91845 on the syringe.
Check for lot codes: 63721060001, 63721070001, 63722020002, 63722030001, 63722040004, 63722090002, 63722100003, 63723020001, 63723060001, 63723090002.
The recall states the syringes have piston sizes that don't match cleared devices, so they may not be safe for intended use.
Check for model number 91845 and lot codes listed: 63721060001, 63721070001, 63722020002, 63722030001, 63722040004, 63722090002, 63722100003, 63723020001, 63723060001, 63723090002.
The recall does not specify a remedy, so no action is required beyond checking if you have the model and lot numbers.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2075-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2075-2024 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.
