CLEARLINK 4C8714Recalls & reported problems
Baxter Healthcare Corporation · Y-Type Blood/Solution Set with Large Standard Blood Filter, 170 to 260 Micron Filter, 2 Luer Activated Valves, Male Luer Lock Adapter · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00085412072982), received between Jan 20, 2023 and Jan 20, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “No Flow” (1 report).
10 other recalls cover devices cleared under the same FDA submission (K993120); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- No Flow1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 20, 2023No Flow; No Flow
IT WAS REPORTED THAT A CLEARLINK BLOODSET WOULD NOT FLOW. THE EVENT OCCURRED DURING AN UNKNOWN PROCESS STEP. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16218860 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K993120. One submission often covers many models, so check the product and lot details in each record.
- Z-0193-05 · Apr 28, 2004 · TerminatedBaxter Clearlink Intravenous (IV) Delivery System; the system consists of solution sets, extension sets and blood sets that have a luer activated valve for IV access, which allows
- Z-1162-03 · Jul 16, 2003 · TerminatedFenwal Y-Type Blood/Solution Set with Large Standard Blood Filter and Pressure Pump, 15 drops/mL, 99'', 170 to 260 Micro Filter, Large Standard Blood Filter, 2 Injection Sites, Mal
- Z-1172-03 · Jul 16, 2003 · TerminatedBaxter Y-Type Blood/Solution Set with Pressure Pump, 10 drops/mL, 99'', Large Standard Blood Filter, 170 to 260 Micron Filter, 2 Injection Sites, Male Luer Lock Adapter, catalog 2C
- Z-1161-03 · Jul 16, 2003 · TerminatedClearlink System Y-Type Blood/Solution Set, 10 drops/mL, 112'', Standard Blood Filter, 170 to 260 Micron Filter, Luer Activated Valve, Male Luer Lock Adapter, catalog 2C8750; Baxte
- Z-1175-03 · Jul 16, 2003 · TerminatedFenwal Straight Type Blood Set with Large Standard Blood filter, 15 drops/mL, 80'', 170 to 260 Micron Filter, Injection Site, Male Luer Lock Adapter, catalog 4C6766; Baxter Healthc
- Z-1176-03 · Jul 16, 2003 · TerminatedFenwal Y-Type Blood/Solution Set with Large Standard Blood Filter, 15 drops/mL, 107'', 2 Injection Sites, Male Luer Lock Adapter, catalog 4C7774; Baxter Healthcare Corporation, Dee
- Z-1178-03 · Jul 16, 2003 · TerminatedFenwal 3-Lead Blood/Solution Set with Large Standard Blood Filter, 15 drops/mL, 82'', 170 to 260 Micron Filter, Injection Site, Male Luer Lock Adapter, catalog 4C7784; Baxter Healt
- Z-1171-03 · Jul 16, 2003 · TerminatedBaxter Y-Type Blood/Solution Set, 10 drops/mL, 115'', 80 Micron Filter, Injection Site, Male Luer Lock Adapter, catalog 2C7617; Baxter Healthcare Corporation, Deerfield, IL 60015 U
- Z-1177-03 · Jul 16, 2003 · TerminatedFenwal Y-Type Blood/Solution Set with Large Standard Blood Filter, 10 drops/mL, 82'', 170 to 260 Micron Filter, Large Bore Tubing, Male Luer Lock Adapter, catalog 4C7776; Baxter He
- Z-1160-03 · Jul 16, 2003 · TerminatedBaxter Y-Type Blood/Solution Set, 10 drops/mL, 112'', Standard Blood Filter, 170 to 260 Micron Filter, Injection Site, Male Luer Lock Adapter, catalog 2C6750; Baxter Healthcare Cor
Other Set, blood transfusion devices
- CLEARLINK 2C8750Baxter Healthcare Corporation · Set, blood transfusion176 reports
- Blood Administration Set V2500B. Braun Medical Inc. · Set, blood transfusion1 recall2 reports
- CLEARLINK 4C8723Baxter Healthcare Corporation · Set, blood transfusion1 death30 reports
- INTERLINK 2C6750HBaxter Healthcare Corporation · Set, blood transfusion18 reports
- INTERLINK 2C6700Baxter Healthcare Corporation · Set, blood transfusion8 reports
- Baxter 2C7627Baxter International Inc. · Set, blood transfusion7 reports
- Blood Administration Set V2400B. Braun Medical Inc. · Set, blood transfusion7 reports
- CLEARLINK 2C8720Baxter Healthcare Corporation · Set, blood transfusion5 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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