Arrow recalls 10cc Luer-Slip Loss of Resistance Syringes (Product Code LR-05501) that may cause dural puncture and require blood patches. Affected lots listed in the recall notice.
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Arrow is recalling 10cc Luer-Slip Loss of Resistance Syringes that could cause dural puncture (a hole in the spinal cord lining) during use, potentially requiring a blood patch. This risk exists in specific production lots.
The syringes may fail during use, creating a hole in the spinal cord lining (dural puncture). This can cause pain, infection, or require a blood patch to seal the hole. The risk is higher during spinal injections.
Healthcare professionals and patients using the recalled syringes for medical procedures. Those with spinal procedures are at higher risk due to potential dural puncture.
Check for the Product Code LR-05501 on the syringe packaging. Affected lots include 13F18J0916 through 13F19K0097 as listed in the recall notice.
Look for the lot numbers listed in the recall notice (13F18J0916 to 13F19K0097) on the syringe packaging.
Reach out to Arrow International Inc. for specific instructions on whether your syringe is affected and what to do next.
Yes, the recall states they may cause dural puncture, which can require a blood patch to treat.
Check the lot number on the syringe packaging against the list provided in the recall notice. If affected, contact Arrow International Inc. for further instructions.
The recall does not mention death as a risk; it states dural puncture and blood patch requirements.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1205-2020 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1205-2020 from Arrow. 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.
