DeRoyal recalls specific surgical tray models due to mislabeled lidocaine containing 0.5% bupivacaine instead of 1% lidocaine. This could cause incorrect medication dosing during procedures.
DeRoyal manufactured certain lots of surgical procedure pack products using Hospira Pfizer 1% Lidocaine which was subsequently recalled due to mislabeling; the product is 0.5% Bupivacaine
DeRoyal is recalling a specific surgical tray model because it contains 0.5% bupivacaine instead of 1% lidocaine. This mislabeling could lead to incorrect medication dosing during medical procedures.
The surgical tray was manufactured with 0.5% bupivacaine instead of the intended 1% lidocaine. This mislabeling could lead to incorrect medication dosing during procedures, potentially causing adverse effects.
Medical professionals using the DeRoyal Pacemaker Tray Pgybk model with lot number 54239375. Patients receiving procedures with this tray may be at risk of incorrect medication dosing.
Check for the model name 'DeRoyal Pacemaker Tray Pgybk' and lot number 54239375. The product was manufactured with an expiration date of 02/01/2022.
Identify the model name and lot number to confirm if your product is affected.
The product contains the wrong medication concentration and may cause incorrect dosing, so it should not be used.
The recall does not specify a remedy, so check with DeRoyal for guidance.
The product expires on 02/01/2022.
We’ve drafted a message you can send DeRoyal to request your refund or repair — edit it as you like.
Subject: Recall Z-1832-2021 — DeRoyal DeRoyal Hello, I own a DeRoyal that is covered by recall Z-1832-2021 from DeRoyal. 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.