Fresenius Medical Care recalls MTS Sets that may have been exposed to freezing temperatures during refrigerated transport, potentially causing damage. Affected units include specific lot numbers and UDI codes. Consumers should check their product details and contact Fresenius for guidance.
Exposed to freezing temperatures due to refrigerated truck malfunctions
Fresenius Medical Care is recalling certain MTS Sets that may have been exposed to freezing temperatures during refrigerated truck transport. This could damage the product, but the recall does not indicate a risk of injury to users.
The MTS Set may have been exposed to freezing temperatures due to refrigerated truck malfunctions. This could cause damage to the product, but the recall does not state that this damage poses a risk of injury to users.
Patients and caregivers using the MTS Set for peritoneal dialysis treatment. Those with specific lot numbers or UDI codes listed in the recall are most at risk.
Check the lot number (20SR08069 or 20PR08237) and UDI code (01)00840861100811 on the product packaging. The MTS Set is a single-use accessory for peritoneal dialysis treatment.
Look for lot numbers 20SR08069 or 20PR08237 and UDI code (01)00840861100811 on the MTS Set packaging.
The recall states the MTS Set may have been exposed to freezing temperatures during refrigerated transport, but it does not indicate a risk of injury to users.
Check the product details for the lot numbers and UDI codes listed in the recall. Contact Fresenius Medical Care for further guidance.
The affected units have lot numbers 20SR08069 or 20PR08237 and UDI code (01)00840861100811.
We’ve drafted a message you can send Fresen:ius to request your refund or repair — edit it as you like.
Subject: Recall Z-2089-2021 — Fresen:ius Fresen:ius Hello, I own a Fresen:ius that is covered by recall Z-2089-2021 from Fresen:ius. 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.
