Exact FDA event identifier

Event 95524

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

Event summary

Timeline bucket: October 23, 2024
Product types: Device
Classifications: Class II
Statuses: Ongoing
Recalling firm wording: Baxter Healthcare Corporation

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

11 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 11

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use in Peritoneal Dialysis

Z-0559-2025

Recall number: Z-0559-2025
Initiated: October 23, 2024
Classification: Class II
Status: Ongoing
Recalling firm: Baxter Healthcare Corporation
Quantity: 409464 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.

Code information

UDI/DI 00085412007731, Lot/Serial Numbers: H23J16074, H23K01082, H23K06107, H23K09093, H23K28051, H23K30081, H23L07053, H23L13051, H23L27093, H24A03061, H24A09035, H24A11064, H24A29132, H24B02038, H24B12086, H24B21079, H24B28090, H24B29072, H24B29098, H24C21093, H24C27090, H24D08064, H24D11050, H24D17040, H24D22081, H24D26058, H24D30076, H24E06065, H24E23037, H24E28051, H24F03045, H24F05065, H24F17086, H24F24033, H24F27036, H24H05061, H24H08032, H24H13040, H24H16043, H24H22025

Distribution pattern

Worldwide distribution.

device · product 2 of 11

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis

Z-0560-2025

Recall number: Z-0560-2025
Initiated: October 23, 2024
Classification: Class II
Status: Ongoing
Recalling firm: Baxter Healthcare Corporation
Quantity: 22392 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.

Code information

UDI/DI 00085412489643, Lot/Serial Numbers: H24C19063, H24G22092, H24G25061

Distribution pattern

Worldwide distribution.

device · product 3 of 11

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis

Z-0561-2025

Recall number: Z-0561-2025
Initiated: October 23, 2024
Classification: Class II
Status: Ongoing
Recalling firm: Baxter Healthcare Corporation
Quantity: 31248 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.

Code information

UDI/DI 00085412476261, Lot/Serial Numbers: H23J13063, H23J26081, H24B18059, H24B19065, H24B19099, H24B20071, H24C18065, H24E22062, H24F11048

Distribution pattern

Worldwide distribution.

device · product 4 of 11

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4483; use in Peritoneal Dialysis

Z-0562-2025

Recall number: Z-0562-2025
Initiated: October 23, 2024
Classification: Class II
Status: Ongoing
Recalling firm: Baxter Healthcare Corporation
Quantity: 62,718

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.

Code information

UDI/DI 00085412007748, Lot/Serial Numbers: H23J10051, H23J23062, H23K20066, H24C08033, H24E16080, H24F12046, H24F17045, H24G02045, H24I02090

Distribution pattern

Worldwide distribution.

device · product 5 of 11

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482; use in Peritoneal Dialysis

Z-0563-2025

Recall number: Z-0563-2025
Initiated: October 23, 2024
Classification: Class II
Status: Ongoing
Recalling firm: Baxter Healthcare Corporation
Quantity: 83,448 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.

Code information

UDI/DI 00085412007748, Lot/Serial Numbers: H23K15033, H23K17088, H23L15049, H23L20049, H24A17046, H24A23069, H24C13090, H24D15036, H24C29493

Distribution pattern

Worldwide distribution.

device · product 6 of 11

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482E; use in Peritoneal Dialysis

Z-0564-2025

Recall number: Z-0564-2025
Initiated: October 23, 2024
Classification: Class II
Status: Ongoing
Recalling firm: Baxter Healthcare Corporation
Quantity: 13,608 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.

Code information

UDI/DI 05413760375861, Lot/Serial Numbers: H23J18054, H24G10063

Distribution pattern

Worldwide distribution.

device · product 7 of 11

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4483; use in Peritoneal Dialysis

Z-0565-2025

Recall number: Z-0565-2025
Initiated: October 23, 2024
Classification: Class II
Status: Ongoing
Recalling firm: Baxter Healthcare Corporation
Quantity: 8,394 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.

Code information

UDI/DI 00085412008783, Lot/Serial Numbers: H23J30067

Distribution pattern

Worldwide distribution.

device · product 8 of 11

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4484; use in Peritoneal Dialysis

Z-0566-2025

Recall number: Z-0566-2025
Initiated: October 23, 2024
Classification: Class II
Status: Ongoing
Recalling firm: Baxter Healthcare Corporation
Quantity: 3204 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.

Code information

UDI/DI 00085412050768, Lot/Serial Numbers: H23J23039

Distribution pattern

Worldwide distribution.

device · product 9 of 11

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number T5C4482; use in Peritoneal Dialysis

Z-0567-2025

Recall number: Z-0567-2025
Initiated: October 23, 2024
Classification: Class II
Status: Ongoing
Recalling firm: Baxter Healthcare Corporation
Quantity: 1496 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.

Code information

UDI/DI 04987456422890, Lot/Serial Numbers: H23L06097, H24A29033

Distribution pattern

Worldwide distribution.

device · product 10 of 11

Baxter MiniCap Extended Life PD Transfer Set (long) with Titanium Spike, Part Number T5C4325K; use in Peritoneal Dialysis

Z-0568-2025

Recall number: Z-0568-2025
Initiated: October 23, 2024
Classification: Class II
Status: Ongoing
Recalling firm: Baxter Healthcare Corporation
Quantity: 1536 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.

Code information

UDI/DI 0085412150710, Lot/Serial Numbers: H24E15066

Distribution pattern

Worldwide distribution.

device · product 11 of 11

Baxter MiniCap Extended Life PD Transfer Set (short) with Titanium Spike, Part Number T5C4326K; use in Peritoneal Dialysis

Z-0569-2025

Recall number: Z-0569-2025
Initiated: October 23, 2024
Classification: Class II
Status: Ongoing
Recalling firm: Baxter Healthcare Corporation
Quantity: 13376 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.

Code information

UDI/DI 0085412150703, Lot/Serial Numbers: H23J02025, H23L04043, H23L05057, H23L05073, H24A29041, H24C01061, H24E13061, H24G15062

Distribution pattern

Worldwide distribution.