The Recall Desk

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.

76–100 of 142

  • HighFDA (Devices)·Z-0615-2026·2025-12-03

    B.Braun IV Administration Sets Recalled for Medication Backflow Risk

    B.Braun IV administration sets used with certain infusion pumps are recalled due to potential medication backflow from secondary containers into primary containers and inability to prime. No illnesses reported.

    Product
    B.BRAUN 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 DROPS/ML,141 in.; Cata
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0708-2026·2025-12-03

    B Braun Medical IV Administration Sets: Medication Backflow and Occlusion Risk

    B Braun Medical Inc is recalling approximately 2,352 Outlook IV administration sets due to potential backflow of medication into primary containers and inability to prime. No injuries have been reported.

    Product
    Outlook 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. OUTLOOK PUMP SET 3 CARESITE LADS 133
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0691-2026·2025-12-03

    B. Braun IV Administration Sets Recalled for Medication Backflow Risk

    B. Braun Medical Inc is recalling 24,072 IV administration sets used with multiple pump models due to potential backflow of medication from secondary containers into primary containers and inability to prime.

    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, 2 CARESITES,
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0645-2026·2025-12-03

    IV Administration Sets Recalled for Potential Medication Backflow and Occlusion Risk

    B Braun Medical Inc recalls 407,800 IV administration sets for potential backflow of medication and occlusion. The defect may prevent proper medication delivery in gravity and pump administration systems.

    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 SET 15DR 5CARESITE 1 ULR
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0649-2026·2025-12-03

    B. Braun IV Administration Sets recalled due to medication backflow risk

    B. Braun IV Administration Sets used with multiple infusion pumps are being recalled due to potential for medication backflow from secondary into primary IV containers and inability to prime properly.

    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/15 DR / mL W
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0702-2026·2025-12-03

    IV Administration Sets Recalled Due to Backflow and Occlusion Risk

    B Braun Medical is recalling IV Administration Sets due to a risk of medication backflow from secondary to primary IV containers and inability to prime. Affected catalog numbers 477002 and 477017 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, 15DR, CARESIT
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0697-2026·2025-12-03

    IV Administration Sets Risk Medication Backflow and Priming Failure

    B Braun Medical IV administration sets used with certain infusion pumps may allow medication to flow backward from secondary containers into primary containers and fail to prime. This could result in incorrect medication delivery.

    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/15 DROPS/ML,
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0617-2026·2025-12-03

    Blood Administration Sets Recalled Due to Medication Backflow and Occlusion Risk

    B Braun Medical Inc recalls 24,624 blood administration sets due to potential medication backflow and priming failures. The defect may allow secondary IV medications to flow backward into primary lines, affecting IV therapy delivery.

    Product
    Blood 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. Y-TYPE BLOOD SET W/ 170
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0637-2026·2025-12-03

    Extension Set Recall: Risk of Medication Backflow in IV Administration

    B Braun Medical is recalling 61,423 extension sets used with IV pumps due to potential backflow of medication and inability to prime. The recalled sets are 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 numbers: 1. ANESTHESIA SET W/ SAFEPORT MANIFOL
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0676-2026·2025-12-03

    IV Administration Set Recalled for Medication Backflow and Priming Issues

    B Braun Medical Inc is recalling IV Administration Sets due to potential backflow of medication from secondary IV containers into primary containers and inability to prime properly.

    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/15 DROPS/ML,
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0705-2026·2025-12-03

    IV Administration Set Risk of Medication Backflow and Occlusion

    B. Braun Medical Inc. recalls AESTHESIA IV Administration Sets due to potential backflow of medication from secondary containers into primary containers and inability to prime. Approximately 4,488 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. AESTHESIA IV SET, 127 in.;
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0616-2026·2025-12-03

    Blood Administration Set Recall Due to Backflow and Occlusion Risk

    B Braun Medical Inc is recalling Blood Administration Sets (catalog 490196) due to potential backflow of medication between IV containers and inability to prime. The recall affects 7,344 units distributed worldwide.

    Product
    Blood 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. Y-TYPE BLOOD SET 124 IN.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0659-2026·2025-12-03

    IV Administration Sets Recalled for Potential Medication Backflow and Occlusion

    B Braun Medical Inc recalls IV administration sets used with its infusion pumps due to potential backflow of medication into primary IV containers and inability to prime.

    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 60 DROP/ML, 10
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0670-2026·2025-12-03

    IV Administration Sets Recalled for Medication Backflow and Priming Failure Risk

    B Braun Medical IV administration sets carry risk of medication backflow into primary containers and inability to prime. Affects approximately 20.7 million 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 15 DR W/2 SAFE
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0632-2026·2025-12-03

    IV Administration Extension Set Recalled Due to Medication Backflow Risk

    B Braun Medical is recalling 13,600 extension sets used in IV administration systems due to potential backflow of medication and inability to prime. The affected product may cause medication to flow back into primary containers.

    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/ B/C VLV, ULTRAPORT, 57 I
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0656-2026·2025-12-03

    IV Administration Sets Recalled for Medication Backflow Risk

    B. Braun Medical Inc is recalling IV Administration Sets used with its infusion pumps due to potential medication backflow from secondary to primary IV containers and inability to prime properly.

    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/15 DROPS/ML
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0639-2026·2025-12-03

    Extension Sets Recalled by B Braun for Medication Backflow Risk

    B Braun Medical Inc is recalling 300 units of extension sets used in IV administration with certain pumps due to potential for medication backflow and inability to prime.

    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/2INJ/FLBL/FML LRLK/CV 34; Catal
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0607-2026·2025-12-03

    FDA Recalls B Braun IV Administration Sets for Medication Backflow Risk

    B Braun Medical Inc recalls 104,784 IV administration sets used with multiple infusion pumps due to potential medication backflow from secondary to primary containers and inability to prime.

    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 W/15 DROPS/ML, 132
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0651-2026·2025-12-03

    IV Administration Set Recalled for Backflow Risk and Occlusion Issues

    B Braun Medical Inc is recalling IV administration sets that may allow medication to flow backward from secondary containers into primary containers and may fail to prime properly.

    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 SET 3 CARESITE ULTRA ZER
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0712-2026·2025-12-03

    IV Administration Sets Recalled for Medication Backflow and Occlusion Risk

    B Braun Medical Inc is recalling 554,015 units of SafeDAY IV administration sets due to potential medication backflow from secondary containers into primary containers and inability to prime the IV line.

    Product
    SafeDAY 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 SET 15 DR W/2 SAFEDAY & STOPCO
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0688-2026·2025-12-03

    IV Administration Sets recalled for potential medication backflow and occlusion risk

    B Braun Medical is recalling IV administration sets that could allow medication backflow from secondary into primary IV containers and may prevent proper priming. The recall affects 28,344 units 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/ B/C VALVE,1
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0629-2026·2025-12-03

    IV Extension Sets Recalled Due to Medication Backflow and Occlusion Risk

    B Braun Medical is recalling extension sets for intravenous administration due to potential medication backflow from secondary containers into primary containers and inability to prime properly. Approximately 2,100 units distributed worldwide are affected.

    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. ANES SET W/DUAL FEM.LL SAFEPORT MAN
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0686-2026·2025-12-03

    IV Administration Set Recalled for Potential Medication Backflow Hazard

    B. Braun Medical's IV administration sets (catalog 490491) are recalled due to potential medication backflow from secondary containers into primary containers and inability to prime (occlusion).

    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 ADMINISTRATION SET, 138
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0709-2026·2025-12-03

    Outlook IV administration sets recalled due to backflow and occlusion risk

    B. Braun Medical is recalling approximately 162,648 Outlook IV administration sets worldwide due to potential medication backflow from secondary into primary IV containers and inability to prime. No injuries or illnesses have been reported.

    Product
    Outlook 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. OUTLOOK IV SET 15DROP W/2 CARESITE; C
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0700-2026·2025-12-03

    B Braun IV Administration Sets Recalled for Potential Backflow Risk

    B Braun Medical Inc recalls IV Administration Sets for potential medication backflow from secondary to primary containers and inability to prime during infusion.

    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. NF1505, IV ADMIN SET W/2 H.
    Category
    Medical Device
    Distribution
    0 states