MEDLINE recalls SYR 10ML L/L WHITE syringes (model 91833) that may not meet FDA clearance standards for size, posing a risk of improper use. Affected units include specific lot codes.
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 WHITE syringes (model 91833) because they may not meet FDA clearance standards for size. This could lead to improper use if the syringes are used for medical purposes.
The syringes may not meet the FDA's clearance standards for their size and configuration. This could lead to improper use if they are intended for medical procedures, but they are designed for single-use without needles.
Users of these syringes for medical purposes, particularly healthcare professionals and patients requiring injections. The risk is low as the syringes are non-sterile and single-use.
Check for the model number 91833 on the syringe packaging. Affected units have specific lot codes: 63720120007, 63721070001, 63721080001, 63721090001, 63721110001, 63722030001, 63722040002, 63722050001, 63722090002, 63722120002, 63723020001, 63723030001, 63723050001, 63723070001.
Look for the model number 91833 on the syringe packaging.
Confirm the syringe lot code matches the listed codes: 63720120007, 63721070001, 63721080001, 63721090001, 63721110001, 63722030001, 63722040002, 63722050001, 63722090002, 63722120002, 63723020001, 63723030001, 63723050001, 63723070001.
These syringes are non-sterile and designed for single-use without needles. They may not meet FDA clearance standards for size, so they should not be used for medical procedures.
Check the model number and lot code to see if your syringes are affected. If they match the listed codes, stop using them and dispose of them safely.
Look for the model number 91833 on the syringe packaging and check if the lot code matches the listed codes.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2065-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2065-2024 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.
