Hazard

Occlusion recalls

142 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all occlusion recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

101–125 of 142

HighFDA (Devices)·Z-0715-2026·2025-12-03
IV Administration Sets Recalled for Medication Backflow and Occlusion Risk
B Braun Medical Inc is recalling Vista IV administration sets due to potential backflow of medication from secondary to primary containers and inability to prime. Approximately 74,652 units were distributed worldwide.
Product
Vista set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. VISTA BASIC PUMP IV SET W/ 15 DROP/ML;
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0689-2026·2025-12-03
IV Administration Set Recalled for Medication Backflow and Priming Failure Risk
B Braun Medical Inc is recalling IV Administration Sets due to potential backflow of medication from secondary to primary IV containers and inability to prime. Approximately 25,728 units were distributed worldwide.
Product
IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET, QUAD MANIFOLD
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0683-2026·2025-12-03
IV Administration Sets Recalled Due to Medication Backflow Risk
B Braun Medical is recalling IV administration sets (Catalog Number 354211) used with their infusion pumps due to potential backflow of medication from secondary containers into primary containers and inability to prime. 286,400 units were distributed worldwide.
Product
IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADM 15 DROP W/3 CARESITE
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0695-2026·2025-12-03
IV Administration Sets recalled for medication backflow and priming problems
B Braun Medical Inc is recalling IV administration sets due to potential medication backflow from secondary to primary containers and inability to prime. The recall affects 111,312 units distributed worldwide.
Product
IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET 15DR HF 4-WAY
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0621-2026·2025-12-03
Burette Set for IV Administration Recalled Due to Backflow Risk
B Braun Medical is recalling 12,320 Burette Sets used in IV administration systems worldwide due to risk of medication backflow and inability to prime the device.
Product
Burette Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. BURETTE SET, 4 CARESITE LADS, STPCK 1
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0662-2026·2025-12-03
IV Administration Set May Cause Medication Backflow and Occlusion
B Braun Medical's IV Administration Sets (catalog 490367) may allow medication from secondary IV containers to flow backward into primary containers and prevent proper priming. The FDA Class II recall affects 6,768 units distributed worldwide.
Product
IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET W/60 DR/ML, CA
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0636-2026·2025-12-03
B Braun IV Extension Set Recalled for Medication Backflow and Occlusion
B Braun Medical Inc is recalling Extension Sets used in IV administration due to potential backflow of medication and inability to prime. Approximately 11,800 units have been distributed worldwide.
Product
Extension Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. EXT SET W/ 6 B/C VALVES, 17 IN; Cat
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0718-2026·2025-12-03
B. Braun IV Administration Sets recalled for potential medication backflow
B. Braun Medical Inc is recalling IV Administration Sets due to potential backflow of medication between containers and possible inability to prime. No injuries have been reported.
Product
IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET, 110 IN.; Cata
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0611-2026·2025-12-03
B Braun IV Administration Sets Recalled for Medication Backflow Risk
B Braun Medical Inc is recalling Anesthesia IV Sets due to potential medication backflow from secondary containers into primary containers and inability to prime. Approximately 19,392 units were distributed worldwide.
Product
Anesthesia IV Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET, 15 DROPS/ML 125 I
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0678-2026·2025-12-03
IV Administration Set Risk of Backflow and Occlusion Recalled
B. Braun Medical recalled 7,008 IV administration sets due to potential backflow of medication from secondary IV containers into primary containers, which could also prevent priming. No injuries have been reported.
Product
IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET 15D, 2 CARESIT
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0644-2026·2025-12-03
B Braun IV Administration Sets Recalled for Medication Backflow Risk
B Braun Medical Inc recalls ULTRASITE IV Administration Sets due to potential medication backflow between containers and inability to prime. Approximately 1,250 units were distributed worldwide.
Product
IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. US1295 ULTRASITE IV ADMIN S
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0653-2026·2025-12-03
IV Administration Set Recalled for Potential Medication Backflow and Priming Failure
B Braun Medical Inc is recalling 18,984 units of IV Administration Sets due to potential backflow of medication from secondary IV lines into primary containers and inability to prime. No adverse events have been reported.
Product
IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET, 81 IN W/ 32 I
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0494-2026·2025-11-19
Nasal Feeding Tubes May Become Occluded, Preventing Nutrition Delivery
Applied Medical Technology's NutraGlide nasal feeding tubes may become occluded, potentially preventing patients from receiving nutrition and medications. The FDA is recalling affected units from lots distributed in Massachusetts, Rhode Island, North Carolina, and Ohio.
Product
Applied Medical Technology, Inc., NutraGlide, 5 f - 6F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0496-2026·2025-11-19
Applied Medical Technology nasal feeding tube may be occluded
Applied Medical Technology is recalling certain NutraGlide nasal feeding tubes that may become occluded, preventing proper nutrition delivery. Patients using affected tubes should discontinue use and contact their healthcare provider.
Product
Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05090-I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0495-2026·2025-11-19
Nasal Feeding Tube May Become Occluded in Applied Medical Technology Device
Applied Medical Technology's NutraGlide nasal feeding tubes may become occluded, potentially blocking nutrient delivery. The FDA is recalling specific lots distributed in four states.
Product
Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-N-I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3173-2024·2024-09-25
Hemodialysis Bloodline Tubing Recall Over Incomplete Connector Insertion Risk
B Braun is recalling SL BLOODLINE FOR FMC 2008 SERIES hemodialysis tubing nationwide due to incomplete connector insertion that may cause blood flow restrictions during treatment.
Product
SL BLOODLINE FOR FMC 2008 SERIES-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2000M2095
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3174-2024·2024-09-25
Hemodialysis tubing may fail to flow if connector is incompletely inserted
B Braun's STREAMLINE FRESENIUS bloodline tubing used in hemodialysis may have a design issue where incomplete insertion of the patient connector prevents proper blood flow during certain procedures. Patients receiving dialysis may experience treatment delays.
Product
STREAMLINE FRESENIUS FOR DAVITA-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2000M2095D
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3178-2024·2024-09-25
Streamline Bloodline Hemodialysis Sets Recalled for Patient Connector Defect
B. Braun is recalling 9,864,165 Streamline Bloodline Sets nationwide due to incomplete patient connector insertion. The defect may restrict fluid flow during hemodialysis and cause therapy delays.
Product
STREAMLINE BLOODLINE SET FOR DIALOG-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2010M2096
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3176-2024·2024-09-25
Hemodialysis bloodline connector insertion defect may cause flow restriction
B Braun Medical is recalling hemodialysis bloodline tubing because the patient connector may not fully insert into the device, potentially blocking blood flow and delaying treatment. Affected units were distributed nationwide.
Product
STREAMLINE BLOODLINE LONG VERSION, FMC-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2000M2095L
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1606-2024·2024-05-01
Alcon Custom Paks Surgical Procedure Packs recalled for cannula defects
Alcon is recalling Custom Paks Surgical Procedure Packs containing Oasis 27Ga Chang Hydrodissection Cannulas due to complaints of particulates, residue, occlusions, and bent tips in sterile cannulas used in ophthalmic surgery.
Product
Various Alcon Custom Paks Surgical Procedure Pack containing Oasis 27Ga Chang Hydrodissection Cannulas. These Custom Paks are surgical procedure packs used by ophthalmic surgeons in a variety of ophthalmic surgeries. The Custom Pak is a collection of various ophthalmic surgical
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1286-2024·2024-04-03
Nimbus II Infusion Pump Systems Recalled for Multiple Potential Device Failures
InfuTronix is recalling 52,328 Nimbus II Infusion Pump Systems due to potential failure modes including battery failure, system errors, drug product leakage, flow rate issues, and housing damage. The devices will no longer be available or supported after June 20, 2024.
Product
Nimbus II Infusion System; Nimbus II PainPRO IT1053; Nimbus II Flex IT1062; Nimbus II Plus IT1078; Nimbus II EpiD IT1124; Nimbus II EMS IT1063; Ambulatory Infusion Pump and components
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2383-2023·2023-08-23
FDA Recalls Dialysis Catheters for Center Lumen Obstruction Risk
Covidien is recalling MAHURKAR dialysis catheters because the center lumen may be blocked by excess silicone lubricant. This could delay treatment and cause blood clots, hemolysis, or embolism.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions REF: 8888345520HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2388-2023·2023-08-23
Dialysis Catheter Recall Due to Center Lumen Occlusion
Covidien is recalling MAHURKAR Triple Lumen Acute Dialysis Catheters due to excessive lubricant blocking the center lumen, which may delay dialysis and cause blood clots. The recall affects 6,949 units distributed in the US and worldwide.
Product
MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, Kit" REF: 8888345629
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2373-2023·2023-08-23
Dialysis Catheter Recall Due to Potential Lumen Occlusion
Covidien LP is recalling MAHURKAR dialysis catheters due to excess silicone lubricant that can block the central lumen, potentially delaying treatment or causing serious complications.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 13 cm, Curved Extensions, PASS Tray REF: 8888103001HP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1310-2023·2023-04-05
Iradimed MRidium MRI Infusion Pump Syringe Adapter Sets Recalled for Occlusion Risk
Iradimed is recalling MRidium MRI 1000 Series Infusion Set Syringe Adapter Sets due to a defective part that can limit venting function and cause occlusion, potentially interrupting medication delivery.
Product
Iradimed Corporation MRidium MRI 1000 Series Infusion Sets, MRI Infusuui Set - Syringe Adapter Set, REF 1057-50,
Category
Medical Device
Distribution
Distributed nationwide