Medical Depot recalls Nitro Glide Knee Walker model 791RD (Red) due to tiller separation risk causing falls. Affected units have serial numbers starting with 21S or UPC 822383019086.
The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury
Medical Depot is recalling Nitro Glide Knee Walkers that may separate at the tiller, causing users to fall. This recall affects people recovering from below-the-knee injuries who use the device for mobility.
The tiller can separate from the base and front caster assembly. If this happens, the user may fall and sustain an injury while trying to move. This hazard occurs during normal use when the device is not properly secured.
Users recovering from below-the-knee injuries who own the Nitro Glide Knee Walker model 791RD (Red) are most at risk. The recall applies to specific serial numbers starting with 21S.
Check for model number 791RD (Red) on the product. Affected units have serial numbers starting with 21S or UPC 822383019086.
Look for model number 791RD (Red) and serial numbers starting with 21S or UPC 822383019086.
The tiller can separate from the base and front caster assembly, causing users to fall and sustain an injury.
Check if your Nitro Glide Knee Walker has model 791RD (Red) and serial numbers starting with 21S or UPC 822383019086. If so, contact Medical Depot for further instructions.
Yes, if the tiller separates, a user may fall and sustain an injury while trying to move.
We’ve drafted a message you can send Medical Depot to request your refund or repair — edit it as you like.
Subject: Recall Z-2355-2024 — Medical Depot Medical Depot Hello, I own a Medical Depot that is covered by recall Z-2355-2024 from Medical Depot. 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.
