FDA recall record

Baxter Healthcare APD Set with Cassette 3-Prong Peritoneal Dialysis Set Indicated for use in recall — FDA Z-1056-2017

Customer complaints received for the presence of leaks

Class IIclassification
Z-1056-2017official record ID
Jan 25, 2017report date

Recall record at a glance

Official recordZ-1056-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBaxter Healthcare Corporation
Report dateJan 25, 2017
Recall initiation dateDec 16, 2016
Quantity8640 eaches
LocationDeerfield, IL, United States

Official product description

APD Set with Cassette 3-Prong Peritoneal Dialysis Set Indicated for use in the treatment of patients with renal failure to provide PD fluid exchanges with Baxter HomeChoice PD systems in clinical and home use settings.

Why the product was recalled

Customer complaints received for the presence of leaks

Distribution information

US only

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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