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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 87998

9 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
April 28, 2021
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Fresenius Medical Care Holdings, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

9 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 9

(1) 08-4078-BB BIBAG 650 GRAMS/BAG 16 BAGS/CASE (2) 08-4080-BB BIBAG 900 grams/bag 12 bags/case For patients with acute and chronic end stage renal disease going under PD in healthcare or home setting GRANUFLO & NATURALYTE: Concentrate is formulated to be used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.

Z-2082-2021
Recall number
Z-2082-2021
Initiated
April 28, 2021
Classification
Class II
Status
Terminated
Quantity
(1) 20 cases (2) 30 cases

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Exposed to freezing temperatures due to refrigerated truck malfunctions

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Exposed to freezing temperatures due to refrigerated truck malfunctions

Code information

(1) Lot Number: B4MA27140 BAG GTIN CASE GTIN BIBAG 650 GRAMS 08-4078-BB 00840861101313 10840861101310 (2) Lot Number: B5MB24110 BAG GTIN CASE GTIN BIBAG 900 GRAMS 08-4080-BB 00840861101320 10840861101327

Distribution pattern

US Distribution to: TX only

device · product 2 of 9

The Drain Bag Set (tubings and flexible bags) is a passive, closed drainage system used as an optional receptacle during an APD treatment. The Drain Bag Set is used to collect effluent in bags rather than letting the effluent flow directly to a drain. The Drain Bag Set connects to the drain line of a cycler set to collect patient effluent by means of gravity and the pumping action of a Peritoneal Dialysis (PD) cycler. The Drain Bag Set connects to the drain line using a standard Luer lock connection. The Drain Bag Set consists of three (3) interconnected 7-liter drain bags, each with a sampling port and an occluding clamp. The tubing lines that connect each drain bag to the drain line have a snap-disconnect tubing segment. This tubing segment allows the user to disconnect individual bags by snapping the tubing apart.

Z-2083-2021
Recall number
Z-2083-2021
Initiated
April 28, 2021
Classification
Class II
Status
Terminated
Quantity
10 cases

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Exposed to freezing temperatures due to refrigerated truck malfunctions

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Exposed to freezing temperatures due to refrigerated truck malfunctions

Code information

Lot Number: 20NR08163 UDI: (01)00840861102037

Distribution pattern

US Distribution to: TX only

device · product 3 of 9

Citrasate Dry Acid Concentrate and GranuFlo Dry Acid Concentrate are each intended to be used as one component in the preparation of dialysate in a 3-stream proportioning hemodialysis machine according to a physician s prescription. Both concentrates are formulated for use in 45X proportioning systems which proportion a nominal ratio of 1 : 1.72 : 42.28 (acid : bicarbonate : water) to generate dialysate. The dialysate is intended to be pumped through a dialyzer, creating an osmotic gradient across the dialyzer membrane to exchange solutes with blood during hemodialysis.

Z-2084-2021
Recall number
Z-2084-2021
Initiated
April 28, 2021
Classification
Class II
Status
Terminated
Quantity
(1) 40 cases (2) 3 cases (3) 4 cases

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Exposed to freezing temperatures due to refrigerated truck malfunctions

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Exposed to freezing temperatures due to refrigerated truck malfunctions

Code information

Lot Number/UDI: (1) 21ATGF013 (01)00884086110135 0FD3251-3B (2) 20SXGF010 (01)00840861101597 0FD3251-3B (3) 20SXGF013 (01)00840861101597

Distribution pattern

US Distribution to: TX only

device · product 4 of 9

026-20036A Liberty Drain Line, Luer Tap For patients with acute and chronic end stage renal disease going under PD in healthcare or home setting

Z-2085-2021
Recall number
Z-2085-2021
Initiated
April 28, 2021
Classification
Class II
Status
Terminated
Quantity
6 Cases

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Exposed to freezing temperatures due to refrigerated truck malfunctions

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Exposed to freezing temperatures due to refrigerated truck malfunctions

Code information

Lot Number: 20HR08054 UDI: (01)00840861101115

Distribution pattern

US Distribution to: TX only

device · product 5 of 9

Citrasate Liquid Acid Concentrate and NaturaLyte Liquid Acid Concentrate are each intended to be used as one component in the preparation of dialysate in a 3-stream proportioning hemodialysis machine according to a physician s prescription. Both concentrates are formulated for use in 45X proportioning systems which proportion a nominal ratio of 1 : 1.72 : 42.28 (acid : bicarbonate : water) to generate dialysate. The dialysate is intended to be pumped through a dialyzer, creating an osmotic gradient across the dialyzer membrane to exchange solutes with blood during hemodialysis.

Z-2086-2021
Recall number
Z-2086-2021
Initiated
April 28, 2021
Classification
Class II
Status
Terminated
Quantity
(1) 1 case (2) 4 cases (3) 5 cases

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Exposed to freezing temperatures due to refrigerated truck malfunctions

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Exposed to freezing temperatures due to refrigerated truck malfunctions

Code information

Lot Number/UDI: (1)21BTAC004 UDI: (01)00840861101535 (2)21AGAC026 UDI: (01)00840861101696 (3)21BTAC008 UDI: (01)00840861101740

Distribution pattern

US Distribution to: TX only

device · product 6 of 9

NaturaLyte Dry Bicarbonate Concentrate is composed of sodium bicarbonate powder and is used as one component in the preparation of dialysate in a 3-stream proportioning hemodialysis machine according to a physician s prescription. NaturaLyte Dry Bicarbonate Concentrate is formulated for use in 45X proportioning systems which proportion a nominal ratio of 1 : 1.72 : 42.28 (acid : bicarbonate : water) to generate dialysate. The dialysate is intended to be pumped through a dialyzer, creating an osmotic gradient across the dialyzer membrane to exchange solutes with blood during hemodialysis.

Z-2087-2021
Recall number
Z-2087-2021
Initiated
April 28, 2021
Classification
Class II
Status
Terminated
Quantity
120 Bags

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Exposed to freezing temperatures due to refrigerated truck malfunctions

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Exposed to freezing temperatures due to refrigerated truck malfunctions

Code information

Lot Number: 21ATBC004 UDI: (01)00840861101955

Distribution pattern

US Distribution to: TX only

device · product 7 of 9

The Fresenius APD Luer-Lock Adapter, Catalog number 050-95018, is designed to connect a peritoneal dialysis bag equipped with a luer-lock connector to a Fresenius Automated Peritoneal Dialysis (APD) cycler set that uses the Fresenius Safe-Lock¿ connector (e.g., Liberty¿ cycler, Newton IQO cycler).

Z-2088-2021
Recall number
Z-2088-2021
Initiated
April 28, 2021
Classification
Class II
Status
Terminated
Quantity
5 cases

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Exposed to freezing temperatures due to refrigerated truck malfunctions

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Exposed to freezing temperatures due to refrigerated truck malfunctions

Code information

Lot Number: 20LR08111 UDI: (01)00840861100811

Distribution pattern

US Distribution to: TX only

device · product 8 of 9

The MTS Set is a single-use, sterile (EO), non-pyrogenic, optional accessory that provides additional connections/disconnections when used with a stay"safe compatible cycler set during acute and chronic PD treatment. The MTS Set utilizes the same PIN engagement technology used in Fresenius stay"safe Patient Connectors (K041792). The MTS Set consists of two (2) stay"safe PIN Connectors at the proximal end, tubing, and a Safe-Lock connector at the distal end. The MTS Set is attached to a cycler set by a patient, care partner, or healthcare professional. The MTS Set is attached during setup to make additional connections to the cycler set when they are prescribed by a physician or when an interruption in treatment is necessary.

Z-2089-2021
Recall number
Z-2089-2021
Initiated
April 28, 2021
Classification
Class II
Status
Terminated
Quantity
5 cases

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Exposed to freezing temperatures due to refrigerated truck malfunctions

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Exposed to freezing temperatures due to refrigerated truck malfunctions

Code information

Lot Number: 20SR08069 UDI: (01)00840861100811 20PR08237 UDI: (01)00840861100811

Distribution pattern

US Distribution to: TX only

device · product 9 of 9

050-95012 Sterile Stay Safe Cap The Indications for Use/Intended Use for the Fresenius Sterile Stay Safe¿ Cap is equivalent to that for the Fresenius Stay Safe Cap and is as follows: Indications for Use Fresenius Sterile Stay Safe¿ Cap is intended to be used for closure of the stay safe peritoneal dialysis connectology system

Z-2090-2021
Recall number
Z-2090-2021
Initiated
April 28, 2021
Classification
Class II
Status
Terminated
Quantity
39 cases

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Exposed to freezing temperatures due to refrigerated truck malfunctions

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Exposed to freezing temperatures due to refrigerated truck malfunctions

Code information

Lot Number: B1ZH191, B1ZI092

Distribution pattern

US Distribution to: TX only