The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

2726–2750 of 52936

  • HighFDA (Devices)·Z-0658-2026·2025-12-03

    IV set 470005 recalled over medication backflow and priming failure

    B. Braun Medical is recalling 29,900 units iv administration sets over the potential for medication backflow from secondary piggyback containers and an 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 SET 15DR 3 CARESITE, 124
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0677-2026·2025-12-03

    IV set 490612 recalled over medication backflow between IV containers

    B. Braun Medical is recalling 5,952 units iv administration sets over the potential for medication backflow from secondary piggyback containers and an 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. 15DR 2SAFELINE 1CARESITE 1S
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0687-2026·2025-12-03

    IV set 490407 recalled over medication backflow between IV containers

    B. Braun Medical is recalling 10,896 units iv administration sets over the potential for medication backflow from secondary piggyback containers and an 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 W/CARESITE EXT
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0696-2026·2025-12-03

    IV set 490437 recalled over piggyback backflow and occlusion risk

    B. Braun Medical is recalling 4,536 units iv administration sets over the potential for medication backflow from secondary piggyback containers and an 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 W/ 15 DROPS/ML
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0671-2026·2025-12-03

    Vented pump sets recalled over medication backflow and occlusion risk

    B. Braun Medical is recalling 12,168 IV administration sets over the potential for medication backflow from secondary piggyback containers and an 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 W/ 15 DROPS/ML
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0703-2026·2025-12-03

    IV set 490301 recalled over backflow from secondary piggyback containers

    B. Braun Medical is recalling 31,392 IV administration sets over the potential for medication backflow from secondary piggyback containers and an 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 AD.SET W/15 DR 128 IN, E
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·25V835000·2025-12-03

    2026 Volkswagen ID.4 and Atlas vehicles recalled for incorrect wheel bolts

    Volkswagen is recalling 27 vehicles with potentially incorrect wheel bolts that could detach during driving. Owners should not drive their vehicles until bolts are inspected and replaced by a dealer at no cost.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID.4, ATLAS CROSS SPORT, ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0610-2026·2025-12-03

    Extension set 490358 recalled over backflow into the primary container

    B. Braun Medical is recalling 1,200 units extension sets over the potential for medication backflow from secondary piggyback containers and an 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, 15D, 144 IN.; Cat
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0672-2026·2025-12-03

    IV set 490519 recalled over piggyback backflow and priming occlusion

    B. Braun Medical is recalling 1,080 IV administration sets over the potential for medication backflow from secondary piggyback containers and an 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 15 DROP, 132 I
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0664-2026·2025-12-03

    IV set 490315 recalled over backflow between primary and secondary containers

    B. Braun Medical is recalling 11,832 IV administration sets over the potential for medication backflow from secondary piggyback containers and an 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, 15 DR/ML,2 CA
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0602-2026·2025-12-03

    Respiratory test panels recalled over elevated risk of false negative results

    BioFire Diagnostics is recalling 23 kits of the BioFire Respiratory Panel 2.1 because unintended movement of pouch chemistry may cause false negative results and control failures.

    Product
    BioFire Respiratory Panel 2.1, IVD, REF: 423742 (30 test kit)
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-0712-2026·2025-12-03

    SafeDAY set 352646 recalled over backflow and priming occlusion

    B. Braun Medical is recalling 554,015 SafeDAY sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.

    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-0643-2026·2025-12-03

    IV set NF1270A recalled over piggyback backflow and priming occlusion

    B. Braun Medical is recalling 13,870 IV administration sets over the potential for medication backflow from secondary piggyback containers and an 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. NF1270A SAFELINE ANESTHESIA
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0636-2026·2025-12-03

    Extension set 490238 recalled over piggyback backflow and occlusion risk

    B. Braun Medical is recalling 11,800 units extension sets over the potential for medication backflow from secondary piggyback containers and an 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 SET W/ 6 B/C VALVES, 17 IN; Cat
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0697-2026·2025-12-03

    IV set 480231 recalled over backflow from secondary piggyback containers

    B. Braun Medical is recalling 85,176 units iv administration sets over the potential for medication backflow from secondary piggyback containers and an 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 W/15 DROPS/ML,
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0615-2026·2025-12-03

    IV set 490349 recalled over backflow from secondary piggyback containers

    B. Braun Medical is recalling 24,648 IV administration sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.

    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-0660-2026·2025-12-03

    IV set 490343 recalled over piggyback backflow and priming occlusion

    B. Braun Medical is recalling 1,272 units iv administration sets over the potential for medication backflow from secondary piggyback containers and an 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 CARESITE, TR
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0609-2026·2025-12-03

    Anesthesia set 490477 recalled over backflow and inability to prime

    B. Braun Medical is recalling 36,552 units anesthesia iv sets over the potential for medication backflow from secondary piggyback containers and an 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, 134
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0648-2026·2025-12-03

    Administration set 354209 recalled over backflow and inability to prime

    B. Braun Medical is recalling 89,552 IV administration sets over the potential for medication backflow from secondary piggyback containers and an 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 ANES 15DROP W/2 CARESITE
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0659-2026·2025-12-03

    IV set 490242 recalled over backflow into the primary bag

    B. Braun Medical is recalling 129,480 IV administration sets over the potential for medication backflow from secondary piggyback containers and an 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-0702-2026·2025-12-03

    IV set 354208 recalled over medication backflow and priming failure

    B. Braun Medical is recalling 126,050 units iv administration sets over the potential for medication backflow from secondary piggyback containers and an 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, 15DR, CARESIT
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0690-2026·2025-12-03

    IV set 490303 recalled over piggyback backflow and occlusion risk

    B. Braun Medical is recalling 32,304 IV administration sets over the potential for medication backflow from secondary piggyback containers and an 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,3 CARESITE LAD
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0704-2026·2025-12-03

    Infusion sets recalled over backflow from secondary bags into primary

    B. Braun Medical is recalling 122,232 IV administration sets over the potential for medication backflow from secondary piggyback containers and an 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, 129 IN, 3 CAR
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0613-2026·2025-12-03

    Anesthesia set 490476 recalled over piggyback backflow and priming occlusion

    B. Braun Medical is recalling 19,320 units anesthesia iv sets over the potential for medication backflow from secondary piggyback containers and an 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, 2-HIGH FLOW STPCK
    Category
    Medical Device
    Distribution
    0 states