Medline Convenience Kits Syringes Recall
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes TAVR PACK DYNJ69246B ABDOMINAL VASCULAR-LF DYNJ905291
Updated February 27, 2026
Medline Convenience Kits containing 10mL polycarbonate colored syringes are being recalled due to unapproved design changes that were not reviewed by the FDA. Healthcare facilities should stop using these kits and return them to Medline Industries.
Is the Medline Industries, LP recalled? Yes. This product was recalled by FDA on February 27, 2026. Details below.
What is recalled
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes, including but not limited to: TAVR PACK DYNJ69246B, ABDOMINAL VASCULAR-LF DYNJ905291D, ANGIOGRAPHIC PACK DYNJ86769, AORTAGRAM PACK DYNJ26783D, AV FISTULA PACK CHS-LF DYNJ35615G, AV SHUNT PACK-LF DYNJ0842516G, CATHETER PACK DYNJ61926, EP DRAPE PACK-LF DYNJ47645C, EP PACK DYNJ47782G, EPS ACCESSORY PACK DYNJT2201S, HEART FAILURE PACK DYNJ64877B, HYBRID PACK DYNJ65925D, INTERVENTIONAL RAD PACK DYNJ44100M, INTERVENTIONAL RADIOLOGY PACK-LF DYNJ0516014AG, MV-PACEMAKER PACK-LF DYNJ41556F, NEURO RADIOLOGY RICHMOND DYNJ68365D, OR HYBRID-M DYNJ907758D, DYNJ907758F, PACEMAKER DYNJ907960C, PACEMAKER PACK DYNJ42557B, DYNJ61411, DYNJ61411A, DYNJ61411B, DYNJ80160, PACER PACK DYNJ40952B, PERIPHERAL ARTERIOGRAM RAD DYNJ61383B, RADIOLOGY PACK DYNJ54762D, TAVR PACK DYNJ55338B, DYNJ69246A, VASCULAR ACCESS TRAY DYNJ52606F, VASCULAR TRAY DYNJ49802C, VEIN PACK DYNJ57512, DYNJ58063, DYNJ84953.
Am I affected
You're affected if your healthcare facility uses Medline Convenience Kits containing 10mL polycarbonate colored syringes. Check the product kit name and DYNJ model number on your packaging against the list of recalled SKUs.
What to do right now
Stop using these Medline Convenience Kits immediately and contact Medline Industries to return them. Notify your purchasing or supply chain department and medical staff using these kits.
The hazard
Unapproved design changes to the products outside of the 510(k) clearance.
Brands affected
- Source
- FDA
- Category
- Medical Devices
- Recall ID
- fda-Z-1878-2026
- Classification
- Class II
- Recalled
- February 27, 2026
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