State

Indiana product recalls

73,738 recalls have nationwide distribution and so reach Indiana. 9,596 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total: 9,596
Critical: 1,908
Severe: 2,534
Most recent: 2026-10-28

Of the 9,596 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 2,534 (26%) are Severe.

Which agencies issued them

These figures cover only the 9,596 recalls whose distribution notice names Indiana specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32676–32700 of 83334

HighFDA (Devices)·Z-1674-2020·2020-04-15
Beckman Coulter MicroScan PROMPT Inoculation System-D Recalled for Incorrect Wands
Beckman Coulter is recalling 3,472 units of the MicroScan PROMPT Inoculation System-D because they contain incorrect prompt wands, which may cause inaccurate antimicrobial susceptibility test results.
Product
Beckman Coulter MicroScan PROMPT Inoculation System-D, Catalog Number B1026-10D, UDI: 15099590659561 - Product Usage: The Prompt Inoculation System-D is used to standardize inocula for microdilution antimicrobial susceptibility test.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1671-2020·2020-04-15
Abbott ARCHITECT C System Mixer Recall Due to Blade Separation Risk
Abbott is recalling ARCHITECT C System Mixers because the blade may separate from the mixer due to screw and nut failure, leading to inadequate mixing of samples and reagents.
Product
ARCHITECT C System Mixer - Product Usage: The ARCHITECT Clinical Chemistry System is designed to perform automated chemistry tests, utilizing photometry and potentiometric technology. The mixer is a component and it is used on all ARCHITECT Clinical Chemistry systems to mix the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1653-2020·2020-04-15
Biomet Recalls Hip Cement Spacer Molds Due to Cleaning Process Concerns
Biomet, Inc. is recalling 230,001 units of BIOMET StageOne Hip Cement Spacer Molds due to potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne, Hip Cement Spacer Mold w/Reinforcement, 9 X 125 MM, 43 MM, Silicone, Sterile, Item 431207.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1669-2020·2020-04-15
Biomet Recalls Knee Tibial Cement Spacer Molds Due to Cleaning Concerns
Biomet is recalling 230,001 units of StageOne Knee Tibial Cement Spacer Molds because of potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne Knee Tibial Cement Spacer Mold, 80 MM, Silicone, Sterile, Item 433180.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1649-2020·2020-04-15
Biomet Hip Stem Cement Spacer Mold Recalled for Cleaning Process Concerns
Biomet is recalling hip stem cement spacer molds due to potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 11 X 200 MM, Silicone, Sterile, Item 431196.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1663-2020·2020-04-15
Biomet Recalls Knee Spacer Molds Due to Insufficient Cleaning Process
Biomet, Inc. is recalling 230,001 units of StageOne Knee Femoral Cement Spacer Molds due to potentially insufficient cleaning or inadequate process monitoring.
Product
BIOMET StageOne Knee Femoral Cement Spacer Mold, 65 MM, Silicone, Sterile, Item 432165.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1655-2020·2020-04-15
Biomet Recalls Hip Cement Spacer Molds Due to Cleaning Process Concerns
Biomet, Inc. is recalling StageOne Hip Cement Spacer Molds because of a potentially insufficient cleaning process or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne, Hip Cement Spacer Mold w/Reinforcement, 13 X 145 MM, 57 MM, Silicone, Sterile, Item 431213.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1652-2020·2020-04-15
Biomet Recalls Hip Stem Cement Spacer Molds Due to Cleaning Concerns
Biomet, Inc. is recalling specific lots of StageOne Select Hip Stem Cement Spacer Molds due to potentially insufficient cleaning processes or inadequate monitoring.
Product
BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 17 X 200 MM, Silicone, Sterile, Item 431199.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1673-2020·2020-04-15
Beckman Coulter LabPro Data Management System Software Update Recall
Beckman Coulter is recalling 177 LabPro Data Management Systems because a security update caused some computers to fail to restart, potentially delaying microbiology test results.
Product
LabPro Data Management System, UDI: 15099590676872 - Product Usage: The LabPro Data Management System is a Microsoft Windows based software program and is intended to manage both microbial identification (ID) and antimicrobial agent susceptibility testing (AST) data generated…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1691-2020·2020-04-15
Microbiologics QC Sets Recalled for Potential Mislabeling of Fungal Strains
Microbiologics Inc is recalling QC sets that may contain Candida utilis instead of the labeled Trichosporon dermatis.
Product
Microbiologics QC SETS AND PANELS, YST Comprehensive QC Set, REF 5195P, containing Trichosporon dermatis, ATCC 204094, QR Code: (01)70845357030770, (17)200831, (10)5195-04.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1646-2020·2020-04-15
Biomet Recalls Hip Stem Cement Spacer Molds Due to Cleaning Concerns
Biomet, Inc. is recalling 230,001 units of StageOne Select Hip Stem Cement Spacer Molds due to potentially insufficient cleaning processes.
Product
BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 15 X 155 MM, Silicone, Sterile, Item 431193.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1658-2020·2020-04-15
Biomet Shoulder Cement Spacer Mold Recalled for Cleaning Process Concerns
Biomet is recalling StageOne Shoulder Cement Spacer Molds due to potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne, Shoulder Cement Spacer Mold 8 MM, 46 X 18 X 53 MM, Silicone, Sterile, Item 431408.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1659-2020·2020-04-15
Biomet Shoulder Cement Spacer Mold Recalled for Cleaning Process Concerns
Biomet is recalling StageOne Shoulder Cement Spacer Molds due to potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne, Shoulder Cement Spacer Mold 10 MM, 50 X 21 X 57 MM, Silicone, Sterile, Item 431410.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1685-2020·2020-04-15
Baxter Recalls GEM Microvascular Couplers Due to Labeling Mismatch
Baxter Healthcare is recalling GEM Microvascular Anastomotic Coupler Devices because the size labeling on the outer tray may not match the inner tray.
Product
GEM Microvascular Anastomotic Coupler Devices - Product Usage: is intended to be used in the anastomosis of veins and arteries normally encountered in microsurgical procedures only in the peripheral vascular system.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1668-2020·2020-04-15
Biomet Knee Tibial Cement Spacer Mold Recalled for Cleaning Process Concerns
Biomet is recalling 230,001 units of StageOne Knee Tibial Cement Spacer Molds due to potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne Knee Tibial Cement Spacer Mold, 75 MM, Silicone, Sterile, Item 433175.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1664-2020·2020-04-15
Biomet Recalls Knee Spacer Molds Due to Cleaning Process Concerns
Biomet, Inc. is recalling BIOMET StageOne Knee Femoral Cement Spacer Molds because the cleaning process may have been insufficient or inadequately monitored.
Product
BIOMET StageOne Knee Femoral Cement Spacer Mold, 70 MM, Silicone, Sterile, Item 432170.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1640-2020·2020-04-15
Biomet Recalls Hip Cement Spacer Molds Due to Cleaning Process Concerns
Biomet, Inc. is recalling StageOne Hip Cement Spacer Molds because of a potentially insufficient cleaning process or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne Hip Cement Spacer Mold with Insert, 56 MM, Silicone, Sterile, Item 431183.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1645-2020·2020-04-15
Biomet Recalls Hip Stem Cement Spacer Molds Due to Cleaning Concerns
Biomet is recalling 230,001 hip stem cement spacer molds due to potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 13 X 145 MM, Silicone, Sterile, Item 431192.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1662-2020·2020-04-15
Biomet Recalls Knee Spacer Molds Due to Insufficient Cleaning Process
Biomet, Inc. is recalling 230,001 units of StageOne Knee Femoral Cement Spacer Molds due to a potentially insufficient cleaning process or inadequate process monitoring.
Product
BIOMET StageOne Knee Femoral Cement Spacer Mold, 60 MM, Silicone, Sterile, Item 432160.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1648-2020·2020-04-15
Biomet Recalls Hip Stem Cement Spacer Molds Due to Cleaning Concerns
Biomet, Inc. is recalling 230,001 units of StageOne Select Hip Stem Cement Spacer Molds due to potentially insufficient cleaning processes.
Product
BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 9 X 200 MM, Silicone, Sterile, Item 431195.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1651-2020·2020-04-15
Biomet Recalls Hip Stem Cement Spacer Molds Due to Cleaning Concerns
Biomet, Inc. is recalling specific lots of StageOne Select Hip Stem Cement Spacer Molds because of a potentially insufficient cleaning process or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 15 X 200 MM, Silicone, Sterile, Item 431198.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1690-2020·2020-04-15
Microbiologics Recalls KWIK-STIK Trichosporon Dermatis Culture Pack
Microbiologics Inc is recalling KWIK-STIK 2 Pack Trichosporon dermatis cultures because they may contain Candida utilis instead of the labeled organism.
Product
KWIK-STIK 2 Pack Trichosporon dermatis derived from ATCC 204094 (Catalog# 0778P, lot 778-65-3)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1656-2020·2020-04-15
Biomet Hip Cement Spacer Mold Recalled for Cleaning Process Concerns
Biomet is recalling StageOne Hip Cement Spacer Molds due to potentially insufficient cleaning processes and inadequate process monitoring.
Product
BIOMET StageOne, Hip Cement Spacer Mold w/Reinforcement, 17 X 165 MM, 64 MM, Silicone, Sterile, Item 431217.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1639-2020·2020-04-15
Biomet Recalls StageOne Hip Cement Spacer Molds Due to Cleaning Concerns
Biomet is recalling 230,001 units of StageOne Hip Cement Spacer Molds because of potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne Hip Cement Spacer Mold with Insert, 52 MM, Silicone, Sterile, Item 431182.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1650-2020·2020-04-15
Biomet Recalls Hip Stem Cement Spacer Molds Due to Cleaning Concerns
Biomet is recalling 230,001 units of StageOne Select Hip Stem Cement Spacer Molds due to potentially insufficient cleaning processes or inadequate monitoring.
Product
BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 13 X 200 MM, Silicone, Sterile, Item 431197.
Category
Medical Device
Distribution
49 states