MEDLINE 20ml red syringes (model 91835) without needles are recalled due to incorrect size configuration. This may cause improper medical 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 20ml red syringes (model 91835) without needles are being recalled because they don't match the medical devices cleared by the manufacturer. This could lead to incorrect medical use if used with devices that require different syringe sizes.
The syringes have sizes and configurations that don't match the medical devices cleared by the manufacturer. This could lead to incorrect use during medical procedures if the syringes are not compatible with the intended devices.
Healthcare professionals and patients using these syringes for medical procedures. Those with specific lot codes are most at risk.
Check for the model number 91835 on the syringe. Look for lot codes: 63721070001, 63721080001, 63721090001, 63721100001, 63722080002, 63722090002, 63722100003, 63723070001, 63723090002.
Identify the model number (91835) and lot codes listed above to confirm if your syringes are affected.
The recall states these syringes have sizes and configurations that don't match cleared devices, so they may not be safe for medical use.
The recall does not specify a remedy, so check the lot codes to see if your syringes are affected and contact the manufacturer for further instructions.
Look for the model number 91835 and lot codes: 63721070001, 63721080001, 63721090001, 63721100001, 63722080002, 63722090002, 63722100003, 63723070001, 63723090002.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2067-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2067-2024 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.
