MEDLINE recalls 20ml blue syringes (model 91837) that may not meet medical device safety standards due to incorrect size configurations. Consumers should check lot codes 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 20ml blue syringes (model 91837) because they may not meet medical device safety standards. This could lead to improper use in medical procedures if the syringes are not compatible with the intended devices.
The syringes may not match the medical devices they were cleared for, which could cause improper use during procedures. This is due to incorrect size configurations that don't meet regulatory standards.
Medical professionals and patients who use these syringes for single-use procedures. Those with specific medical device compatibility needs are at higher risk.
Check for the model number 91837 on the syringe packaging. Look for lot codes: 63721010004, 63721040002, 63721050002, 63721060001, 63721070001, 63721080001, 63721100001, 63722050001, 63722090002, 63722100003, 63722120002, 63723020001, 63723030001, 63723050001, 63723060001, 63723070001, 63723090002, 63723100003, 63723120002.
Look for lot codes on the syringe packaging: 63721010004, 63721040002, 63721050002, 63721060001, 63721070001, 63721080001, 63721100001, 63722050001, 63722090002, 63722100003, 63722120002, 63723020001, 63723030001, 63723050001, 63723060001, 63723070001, 63723090002, 63723100003, 63723120002.
The recall states these syringes may not meet medical device safety standards, so they should not be used for medical procedures.
Check the lot code on the syringe packaging. If it matches the listed codes, contact MEDLINE for further instructions.
Look for the model number 91837 and the specific lot codes listed in the recall notice.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2069-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2069-2024 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.
