Wellspect HealthCare recalls certain LoFric Origo urinary catheters with a potential defect in the distal tip. Affected units include Lot #450422. Consumers should contact Wellspect for details.
Wellspect Healthcare is voluntarily recalling certain LoFric¿ Origo" urethral catheters due to a potential defect which may be present in the catheters distal tip.
Wellspect HealthCare is recalling specific LoFric Or:16in, FR12 urinary catheters due to a potential defect in the catheter's distal tip. This defect could lead to complications during use, so affected users should stop using the product and contact Wellspect for guidance.
The catheter's distal tip may have a defect that could cause complications during use. This defect might lead to issues such as improper placement or injury if the catheter is not functioning correctly.
Patients using the recalled LoFric Origo catheters are most at risk. The recall applies to Lot #450422 units sold under the Wellspect HealthCare brand.
Check for the product name 'LoFric Origo', model 'Tiemann', length '16in', and size 'FR12'. Affected units are Lot #450422.
Identify the product name, model, length, and size to confirm if it matches the recalled units.
Reach out to Wellspect HealthCare for specific instructions on how to handle the recalled product.
The recall states there is a potential defect in the catheter's distal tip, but does not specify the exact nature of the defect.
Check for the product name 'LoFric Origo', model 'Tiemann', length '16in', and size 'FR12' with Lot #450422.
Contact Wellspect HealthCare for specific instructions on how to handle the recalled product.
We’ve drafted a message you can send Wellspect HealthCare to request your refund or repair — edit it as you like.
Subject: Recall Z-2644-2020 — Wellspect HealthCare Wellspect HealthCare Hello, I own a Wellspect HealthCare that is covered by recall Z-2644-2020 from Wellspect HealthCare. 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.
