State

Indiana product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40176–40200 of 83407

HighFDA (Devices)·Z-0445-2019·2018-11-21
Luminex Recalls Verigene Blood Culture Gram-Positive Nucleic Acid Kits
Luminex Corporation is recalling 12,700 trays of Verigene Blood Culture Gram-Positive Nucleic Acid Kits due to a potential for false negative results.
Product
VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as five-pack carriers) Product Usage: In vitro diagnostic test for the simultaneous detection and identification of potentially pathogenic gram-positive bacteria.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0435-2019·2018-11-21
AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications after 18 months.
Product
OviTex 2S Reinforced BioScaffold 10x12cm, Part Number F10258-1012G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0432-2019·2018-11-21
AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold mesh devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex 2S Reinforced BioScaffold 18x22cm, Part Number F10258-1822G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0469-2019·2018-11-21
Tosoh AIA-900 Analyzer Recalled Due to Pickup Arm Malfunction
Tosoh Bioscience is recalling 393 AIA-900 Analyzers because a pickup arm malfunction can stop the device from testing patient samples, causing delays in results.
Product
AIA-900 Analyzer, Product code 022930, 022930R
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0449-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect
Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail Left 130 Deg 11x300mm, Item Number 814611300 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0430-2019·2018-11-21
AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold devices because the suture material may degrade, causing them to fail burst specifications.
Product
OviTex 2S Reinforced BioScaffold 10x20cm, Part Number F10258-1020G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0424-2019·2018-11-21
AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold mesh devices because the suture material degraded, causing some units to fail burst specifications.
Product
OviTex 1S Reinforced BioScaffold 10x20cm, Part Number F10256-1020G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0421-2019·2018-11-21
AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold 4x8cm devices because the PGA suture material degraded, causing the devices to fail burst specifications.
Product
OviTex 1S Reinforced BioScaffold 4x8cm, Part Number F10256-0408G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0418-2019·2018-11-21
AROA Biosurgery Recalls OviTex Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex Reinforced BioScaffold mesh devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex Reinforced BioScaffold 10x20cm, Part Number F10254-1020G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0427-2019·2018-11-21
AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex 1S Reinforced BioScaffold 20x20cm, Part Number F10256-2020G
Category
Medical Device
Distribution
8 states
HighFDA (Food)·F-0622-2019·2018-11-21
Rojo's Autentico Black Bean 5 Layer Dip Recalled for Contamination Risk
Simply Fresh Foods is recalling Rojo's Autentico Black Bean 5 Layer Dip due to potential Salmonella or Listeria monocytogenes contamination in the corn.
Product
Rojo's Autentico Black Bean 5 Layer Dip; Layers of Black Beans, Guacamole, Salsa, sour Cream and Cheddar Cheese. NET WT. 40 oz. (2 Lbs. 9 oz.) 1.13 kg UPC: 047502 441269 Simply Fresh Foods, Inc., Buena Park, Ca 9-620 WWW Rojossalsa.com
Category
Food
Distribution
12 states
HighFDA (Devices)·Z-0416-2019·2018-11-21
AROA Biosurgery Recalls OviTex Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex Reinforced BioScaffold mesh devices because the suture material degraded, causing some units to fail burst specifications.
Product
OviTex Reinforced BioScaffold 6x10cm, Part Number F10254-0610G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0428-2019·2018-11-21
AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Devices
AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex 2S Reinforced BioScaffold 6x10cm, Part Number F10258-0610G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0419-2019·2018-11-21
AROA Biosurgery Recalls OviTex Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex Reinforced BioScaffold 16x20cm devices because the suture material degraded, causing them to fail burst specifications after 18 months.
Product
OviTex Reinforced BioScaffold 16x20cm, Part Number F10254-1620G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0423-2019·2018-11-21
AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex 1S Reinforced BioScaffold 10x12cm, Part Number F10256-1012G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0431-2019·2018-11-21
AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications after 18 months.
Product
OviTex 2S Reinforced BioScaffold 16x20cm, Part Number F10258-1620G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0452-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Issue
Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail 125 Deg 12x165mm, Item Number 816712165 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0447-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Issue
Zimmer Biomet is recalling 2,163 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail Left Deg 9x300mm, Item Number 814609300 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0411-2019·2018-11-21
GE Healthcare Recalls Aisys Anesthesia Systems for Missing Backup Ventilation Feature
GE Healthcare is recalling Aisys anesthesia systems because a software upgrade prevents the device from automatically switching to backup ventilation if a patient stops breathing.
Product
Aisys Anesthesia System. Sold under the following product names: AISYS, AISYS 10.X TO 11.X UPGRADE KIT DUTCH, AISYS 10.X TO 11.X UPGRADE KIT ENGLISH, AISYS 10.X TO 11.X UPGRADE KIT ENGLISH FOR USA, AISYS 10.X TO 11.X UPGRADE KIT FRENCH, AISYS 10.X TO 11.X UPGRADE KIT GERMAN…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0453-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect
Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail 130 Deg 10x165mm, Item Number 816810165 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0434-2019·2018-11-21
AROA Biosurgery Recalls OviTex Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex Reinforced BioScaffold 18x22cm devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex Reinforced BioScaffold 18x22cm, Part Number F10254-1822G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0461-2019·2018-11-21
Medtronic Recalls Parietex Composite Parastomal Mesh Due to Failure Reports
Medtronic is voluntarily removing Parietex Composite Parastomal Mesh from the market after receiving reports of product failure leading to hernia recurrence.
Product
Parietex Composite Parastomal Mesh (Product Number PCOPM15 / PCOPM20) Product Usage: The PCOPM15 and PCOPM20 reorder codes are circular in shape, made from a three-dimensional monofilament polyester fabric with a two-dimensional monofilament polyester central band. One side…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0420-2019·2018-11-21
AROA Biosurgery Recalls OviTex Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex Reinforced BioScaffold 20x20cm devices because the suture material degraded, causing them to fail burst specifications after 18 months.
Product
OviTex Reinforced BioScaffold 20x20cm, Part Number F10254-2020G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0454-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Issue
Zimmer Biomet is recalling 2,163 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail 130 Deg 12x165mm, Item Number 816812165 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0429-2019·2018-11-21
AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold 10x12cm devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex 2S Reinforced BioScaffold 10x12cm, Part Number F10258-1012G
Category
Medical Device
Distribution
8 states