The Recall Desk

Hazard

Injection Failure recalls

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

What the numbers show

Total
8
Critical
0
Severe
0
Most recent
2024-11-27

Of the 8 injection failure recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all injection failure 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.

1–8 of 8

  • HighFDA (Devices)·Z-0468-2025·2024-11-27

    Posi-Stop Injection Needles Recalled for Manufacturing Debris Blocking Flow

    Hobbs Medical is recalling Posi-Stop Injection Needles because manufacturing debris blocks the needle, preventing injection solutions from flowing properly. The 70 affected units were distributed to healthcare facilities in multiple U.S. states and Canada.

    Product
    Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4720
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0474-2025·2024-11-27

    Posi-Stop Injection Needles Recalled Due to Manufacturing Debris Blocking Injection Flow

    Hobbs Medical recalls Posi-Stop injection needles because manufacturing debris can block the needle, preventing injection solutions from flowing properly. Affected units were distributed across multiple US states and Canada.

    Product
    Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4718
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0476-2025·2024-11-27

    FDA Recalls Posi-Stop Injection Needles Due to Manufacturing Debris

    Hobbs Medical is recalling Posi-Stop Injection Needles (25 gauge) because some units contain debris in the needle shaft that blocks injection solution flow.

    Product
    Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0471-2025·2024-11-27

    Injection Needles Recalled for Manufacturing Debris Blocking Medication Flow

    Hobbs Medical is recalling Posi-Stop Injection Needles due to manufacturing debris inside the needle shaft that blocks medication flow. The affected lot was distributed across multiple US states and Canada.

    Product
    Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4716
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0472-2025·2024-11-27

    Posi-Stop Injection Needle Recalled Due to Manufacturing Debris Blockage

    Hobbs Medical is recalling Posi-Stop Injection Needles (23 Gauge, Lot H11-23-057) because some units contain manufacturing debris that blocks the needle opening, preventing injection solutions from flowing properly.

    Product
    Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4721
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0470-2025·2024-11-27

    Posi-Stop Injection Needle Recall Due to Manufacturing Debris

    Hobbs Medical is recalling Posi-Stop Injection Needles (23 Gauge, Catalog 4706) due to manufacturing debris in the inner sheath that can block the needle and prevent injection solution flow.

    Product
    Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4706
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2624-2016·2016-08-31

    Siemens CT Scanner Recall Due to Contrast Injection Failure

    Siemens is recalling one SOMATOM Definition AS CT scanner because a software error prevents the automatic injection of contrast agent during scans.

    Product
    SOMATOM Definition AS with software version VA48A-SP2; Model # 10430603, computed tomography x-ray system
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Drugs)·D-0956-2016·2016-06-15

    Novo Nordisk Recalls Norditropin Pens Due to Delivery System Defect

    Novo Nordisk is recalling 723 Norditropin FlexPro pens due to a potential assembly fault that may cause the pen to block during the air shot step.

    Product
    NORDITROPIN — NORDITROPIN (SOMATROPIN)
    Category
    Drug
    Distribution
    Distributed nationwide