Fresenius Liberty Cycler-Peritoneal Dialysis Cycler recall
Fresenius Liberty Cycler-Peritoneal Dialysis Cycler Model: 180111 and RTLR180111
Why was Fresenius Liberty Cycler-Peritoneal Dialysis Cycler recalled?
The door latch may not fully close and the door may open unexpectedly. The door may make physical contact with anything near the door of the machine, including the patient. May cause injury, delay in treatment, or Increased Intraperitoneal Volume (IIPV) (overfill).
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
All lot numbers
- Product
- Fresenius Liberty Cycler-Peritoneal Dialysis Cycler Model: 180111 and RTLR180111
- Recalling firm
- Fresenius Medical Care Renal Therapies Group, LLC
- Quantity
- 14,094 units
- Distribution
- Nationwide Distribution
- Recall date
- February 3, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)