Epimed recalls Versa Kath Mini Kit with incorrect catheter size labeling. The kit includes a 21-gauge catheter but labels state 12-gauge. This could lead to improper use during epidural anesthesia procedures.
Mislabeled - The product's labeling contains an incorrect size for the catheter included in the kit. The kit contains a 21 gauge catheter, however the labeling states a 12 gauge catheter is included.
Epimed is recalling its Versa Kath Mini Kit because the product labels incorrectly state it includes a 12-gauge catheter when it actually contains a 21-gauge catheter. This mislabeling could lead to improper catheter use during epidural or caudal anesthesia procedures, potentially causing complications.
The kit contains a 21-gauge catheter but the labeling states it includes a 12-gauge catheter. This mismatch could lead to improper catheter size selection during medical procedures, potentially causing complications like incorrect insertion depth or tissue damage.
Healthcare professionals using the Versa Kath Mini Kit for epidural or caudal anesthesia procedures are likely affected. Patients receiving these procedures may be at risk if the catheter size is misused due to incorrect labeling.
Check for the product code REF 181-2112, RX, (01) on the kit. The kit includes a 21-gauge catheter but labels state a 12-gauge catheter is included. This product was sold for epidural or caudal anesthesia procedures.
Verify the catheter size listed on the product label matches the actual catheter included (21-gauge instead of 12-gauge).
The product's labeling incorrectly states it includes a 12-gauge catheter when it actually contains a 21-gauge catheter.
The kit contains a 21-gauge catheter, not a 12-gauge catheter as labeled.
Look for the product code REF 181-2112, RX, (01) on the kit. The kit includes a 21-gauge catheter but labels state a 12-gauge catheter is included.
We’ve drafted a message you can send Epimed to request your refund or repair — edit it as you like.
Subject: Recall Z-2068-2019 — Epimed Epimed Hello, I own a Epimed that is covered by recall Z-2068-2019 from Epimed. 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.
