The Recall Desk

State

Indiana product recalls

73,824 recalls have nationwide distribution and so reach Indiana. 9,598 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,598
Critical
1,908
Severe
2,536
Most recent
2026-11-04

Of the 9,598 recalls naming Indiana we have scored against our rubric, 1,908 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,536 (26%) are Severe.

Which agencies issued them

These figures cover only the 9,598 recalls whose distribution notice names Indiana specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48851–48875 of 83422

  • ModerateFDA (Devices)·Z-1908-2017·2017-05-10

    Breg Recalls If Hip Sterile Polar Dressings Due to Unsealed Pouches

    Breg Inc is recalling 2,609 units of If Hip Sterile Polar Dressings because some may have unsealed pouches, rendering them non-sterile.

    Product
    If Hip, Sterile Polar Dressing P/N 10680 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy pad and the skin. Sterile dressings are typically applied in a non-sterile environment after post-op and on occasion…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1983-2017·2017-05-10

    Anspach Effort Pediatric Craniotome Recalled for Missing Service Interval

    The Anspach Effort, Inc. is recalling three Pediatric Craniotomes because the supplied directions for use did not contain a recommended service interval.

    Product
    PEDIATRIC CRANIOTOME, BM Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2011-2017·2017-05-10

    Anspach Effort Recalls Minimal Access Straight Driver for Missing Service Interval

    The Anspach Effort, Inc. is recalling 98 Minimal Access Straight Drivers because the supplied directions for use did not contain a recommended service interval.

    Product
    Minimal Access Straight Driver Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2021-2017·2017-05-10

    Anspach Effort Recalls 10.5cm QD Angle Attachment for Pneumatic Systems

    The Anspach Effort, Inc. is recalling 203 units of the 10.5cm QD Angle Attachment because the supplied directions for use did not contain a recommended service interval.

    Product
    10.5cm QD Angle Attachment Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1946-2017·2017-05-10

    Anspach Effort Electronic Foot Control Recalled for Missing Service Interval

    The Anspach Effort, Inc. is recalling 207 Electronic Foot Controls because the supplied directions for use did not contain a recommended service interval.

    Product
    Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2001-2017·2017-05-10

    Anspach Pneumatic Attachment Recalled for Missing Service Interval Instructions

    The Anspach Effort, Inc. is recalling 9,829 pneumatic attachments because the supplied directions for use did not include a recommended service interval.

    Product
    12.4cm Heavy Duty Long Heavy Short Attachment Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1951-2017·2017-05-10

    Anspach Effort Recalls eMax2 Hybrid Hand Control for Missing Service Interval

    The Anspach Effort, Inc. is recalling 293 eMax2 Hybrid Hand Controls because the supplied directions for use did not contain a recommended service interval.

    Product
    eMax2 Hybrid Hand Control Product Usage: Electric system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0695-2017·2017-05-10

    Fagron Recalls Zinc Oxide Paste Due to Labeling Error

    Fagron, Inc. is recalling Zinc Oxide Paste 25% because of an incorrect strength value in the Drug Facts Panel.

    Product
    Zinc Oxide Paste 25%, 500 g, For Prescription Compounding, Fagron Inc.2400 Pilot Knob Rd, St. Paul, MN 55120m NDC 51522-0694-5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1941-2017·2017-05-10

    Anspach Effort Recalls BLACKMAX-NEURO Pneumatic System for Missing Service Interval

    The Anspach Effort, Inc. is recalling 25 BLACKMAX-NEURO LOW PRESSURE pneumatic systems because the supplied directions for use did not include a recommended service interval.

    Product
    BLACKMAX-NEURO LOW PRESSURE Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2028-2017·2017-05-10

    Anspach Effort J-Latch Recall for Missing Service Interval Instructions

    The Anspach Effort, Inc. is recalling 16 Small Attachment, J-Latch units because the supplied directions for use did not contain a recommended service interval.

    Product
    SMALL ATTACHMENT, J-LATCH
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1892-2017·2017-05-10

    Zimmer TM Ardis Interbody System Recalled for Procedural Error in Literature Approval

    Zimmer Trabecular Metal Technology, Inc. is recalling the TM Ardis Interbody System due to a procedural error in the approval of literature, resulting in the unauthorized release of certain content.

    Product
    The TM Ardis Interbody System implant is a convex, straight TLIF or PLIF device for interbody fusion of the anterior column of the spine. TM Ardis is designed for fusing the adjacent bony surfaces and may be used to replace a disc at one or two contiguous levels in L2-S1. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0692-2017·2017-05-10

    Aripiprazole Tablets Recalled for Out-of-Specification Assay Results

    The Harvard Drug Group is recalling Aripiprazole Tablets, 2 mg, due to out-of-specification assay results. The recall covers 36,990 tablets distributed nationwide and in Puerto Rico.

    Product
    Aripiprazole Tablets, 2 mg, 30 count unit dose box, Rx only, Manufactured by Apotex Inc., Toronto, Ontario, Canada, Distributed by Major Pharmaceuticals, Livonia, MI NDC 0904-6509-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1949-2017·2017-05-10

    Anspach Effort Recalls Electronic Foot Controls Due to Missing Service Interval

    The Anspach Effort, Inc. is recalling 821 Electronic Foot Controls because the supplied directions for use did not contain a recommended service interval.

    Product
    Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system
    Category
    Medical Device
    Distribution
    Distributed nationwide