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.

42501–42525 of 83407

SevereFDA (Food)·F-1625-2018·2018-07-11
Caito Foods Recalls Honeydew and Cantaloupe for Salmonella Risk
Caito Foods Service, Inc. is recalling honeydew and cantaloupe products due to potential Salmonella contamination. The recall covers approximately 3.16 million pounds distributed across 23 states.
Product
Honeydew, Clear Generic Label Distributed by Caito Foods; distributed at Gordon Food Service, Clear Generic Label Distributed by Caito Foods Distributed at Kroger with Clear Generic Label Distributed by Renaissance Food Group Distributed at SpartanNash Distribution…
Category
Food
Distribution
23 states
SevereFDA (Food)·F-1628-2018·2018-07-11
Caito Foods Recalls Multiple Brands of Mixed Melon for Salmonella Risk
Caito Foods Service, Inc. is recalling mixed melon products sold under various brands due to potential Salmonella contamination.
Product
Multiple Brands Mixed Melon: Customer Product Description Pack Weight UPC Label Description/Brand Caito Foods Disribution FRUIT SNACK TRAY 3/32Z, 32 oz., UPC: 81851301454 Clear Generic Label Distributed by Caito Foods Caito Foods…
Category
Food
Distribution
23 states
SevereFDA (Devices)·Z-2351-2018·2018-07-11
FHC Depth Stop Adapter Recalled for Potential Lead Damage
FHC, Inc. is recalling the Depth Stop Adapter because over-tightening the screw can damage the implanted lead, requiring removal and replacement.
Product
microTargeting" STar" Drive System (Manual), Product Number 70-ZD-MA
Category
Medical Device
Distribution
46 states
SevereNHTSA·18V461000·2018-07-11
Lamborghini Recalls 2015-2016 Aventador Models for Wheel Detachment Risk
Lamborghini is recalling 2015-2016 Aventador SV vehicles because loose brake disc bolts may cause wheels to detach, increasing crash risk.
Product
LAMBORGHINI — LAMBORGHINI AVENTADOR, AVENTADOR ROADSTER
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-1642-2018·2018-07-11
Caito Foods Recalls Mixed Melon Products for Salmonella Risk
Caito Foods Service, Inc. is recalling multiple brands of mixed melon products due to potential Salmonella contamination. The recall affects approximately 3.16 million pounds of product distributed across 23 states.
Product
Multiple Brands Mixed Melon: Customer Product Description Pack Weight UPC Label Description/Brand Walmart SALAD SEASONAL FRUIT 4/10Z 13 oz., UPC: 826766254262 Freshness Guaranteed label
Category
Food
Distribution
23 states
HighFDA (Devices)·Z-2342-2018·2018-07-11
Beaver Visitec Safety Sideport Knife Blades May Detach During Surgery
Beaver Visitec is recalling Safety Sideport Knives because blades may fall out of handles due to non-cured epoxy. The defect poses a risk during ophthalmic surgery.
Product
Safety Sideport Knife 1.0mm 45¿, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surgery
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V464000·2018-07-11
Volkswagen Recalls 2015-2018 Golf Models for Ignition Key Removal Defect
Volkswagen is recalling 2015-2018 Golf and Golf Sportwagen vehicles because silicate buildup may allow the key to be removed while the car is not in Park, increasing rollaway risk.
Product
VOLKSWAGEN — VOLKSWAGEN GOLF, GOLF SPORTWAGEN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2295-2018·2018-07-11
Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation Complaints
Howmedica Osteonics Corp. is recalling specific lots of LFIT Anatomic CoCr Femoral Heads due to higher-than-expected complaints of femoral head/hip stem disassociation.
Product
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-136
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·18753·2018-07-11
Burton Recalls Snowboard Boots Due to Unexpected Binding Release Hazard
Burton is recalling about 4,800 Step On snowboard boots because they can unexpectedly release from bindings, posing a fall hazard. No injuries have been reported.
Product
Snowboard boots
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2292-2018·2018-07-11
Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation
Howmedica Osteonics Corp. is recalling specific LFIT Anatomic CoCr Femoral Heads because of a higher than expected number of complaints regarding disassociation from the hip stem.
Product
LFIT Anatomic CoCr Femoral Heads, 6260-9-036
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V462000·2018-07-11
KZRV Recalls 2018-2019 Sportsmen Trailers Due to Propane Leak Risk
KZRV is recalling 2018-2019 Sportsmen recreational trailers because propane gas may leak at the outside kitchen cooktop, increasing fire risk.
Product
KZRV — KZRV SPORTSMEN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2299-2018·2018-07-11
Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation
Howmedica Osteonics Corp. is recalling LFIT Anatomic CoCr Femoral Heads due to a higher than expected number of complaints about disassociation from the hip stem.
Product
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-236
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2296-2018·2018-07-11
Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation
Howmedica Osteonics Corp. is recalling specific lots of LFIT Anatomic CoCr Femoral Heads due to a higher than expected number of complaints about femoral head and hip stem disassociation.
Product
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-140
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2297-2018·2018-07-11
Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation
Howmedica Osteonics Corp. is recalling specific lots of LFIT Anatomic CoCr Femoral Heads due to a higher than expected number of complaints about femoral head and hip stem disassociation.
Product
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-144
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V460000·2018-07-11
Jayco Recalls 2018 Octane Travel Trailers Due to Missing Generator Exhaust Pipe
Jayco is recalling 2018 Octane travel trailers with optional generators because a missing exhaust pipe may allow exhaust to enter the trailer, increasing injury risk.
Product
JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER OCTANE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2298-2018·2018-07-11
Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation
Howmedica Osteonics Corp. is recalling LFIT Anatomic CoCr Femoral Heads because of a higher than expected number of complaints regarding disassociation from the hip stem.
Product
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-336
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2353-2018·2018-07-11
FHC Depth Stop Adapter Recall Due to Lead Damage Risk
FHC, Inc. is recalling microTargeting Lead Adapters because over-tightening the depth stop screw can damage the lead and stylet, potentially requiring surgical replacement.
Product
microTargeting" Lead Adapter for microTargeting" Drive, Product Number 66-CN-DB
Category
Medical Device
Distribution
46 states
HighFDA (Devices)·Z-2341-2018·2018-07-11
Intuitive Surgical Recalls da Vinci X Systems with Defective Arm Controller Boards
Intuitive Surgical is recalling 35 da Vinci X Surgical Systems because defective Arm Controller Joint boards have a high rate of failure.
Product
da Vinci X Surgical System, Model IS4200. Product Usage: The Intuitive Surgical Endoscopic Instrument Control System (da Vinci X Surgical System Mode IS4200) is intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments including rigid…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V465000·2018-07-11
BMW and MINI Recall 5,309 Vehicles for Crankshaft Sensor Defect
BMW is recalling 5,309 vehicles because a crankshaft sensor firmware error may cause the engine to stall, increasing crash risk.
Product
MINI — MINI, BMW JCW, X2, COUNTRYMAN, CLUBMAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2337-2018·2018-07-11
Terumo Recalls Angio-Seal Evolution Vascular Closure Devices
Terumo Medical Corp is recalling 240 Angio-Seal Evolution Vascular Closure Devices because they were released before required validation was completed.
Product
Angio-Seal Evolution Vascular Closure Device, Cat. No. C610135
Category
Medical Device
Distribution
12 states
HighFDA (Devices)·Z-2294-2018·2018-07-11
Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation
Howmedica Osteonics Corp. is recalling specific lots of LFIT Anatomic CoCr Femoral Heads due to a higher than expected number of complaints about femoral head and hip stem disassociation.
Product
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-044
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2357-2018·2018-07-11
FHC Depth Stop Adapter Recall for Lead Damage Risk
FHC, Inc. is recalling the microTargeting STar Drive System (Manual) because the Depth Stop Adapter can damage implanted leads if over-tightened, requiring replacement.
Product
microTargeting" STar" Drive System (Manual) Distributed by Medtronic, Product Number FC8001
Category
Medical Device
Distribution
46 states
ModerateFDA (Devices)·Z-2334-2018·2018-07-11
St. Jude Medical Confirm Rx Insertable Cardiac Monitor Recall
St. Jude Medical is recalling 986 Confirm Rx Insertable Cardiac Monitors because exposure to sub-freezing temperatures caused a transient battery voltage drop, resulting in an incorrect low battery indicator display.
Product
St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor, Sterile EO, Model #: DM3500 The Confirm Rx ICM is indicated for the monitoring and diagnostic evaluation of patients who experience unexplained symptoms such as: dizziness, palpitations, chest pain, syncope, and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2344-2018·2018-07-11
Ortho-Clinical Diagnostics Recalls VITROS Chemistry Products PHYT Slides
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products PHYT Slides due to a potential for imprecise results in quality control and patient samples.
Product
VITROS Chemistry Products PHYT Slides, Catalog Number 8298671. in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2335-2018·2018-07-11
St Jude Medical Recalls Merlin PCS Programmer Software for ICM Battery Display Error
St Jude Medical is recalling Merlin PCS Programmer Software to address an incorrect low battery indicator on Confirm Rx ICM devices caused by supply chain temperature exposure.
Product
Merlin PCS Programmer Software: 3330 The Merlin PCS programmer (model 3650) is a portable, external device used to support the implanted device, and for this recall the software that resides on the programmer (software model 3330) is the method of delivery of the new…
Category
Medical Device
Distribution
Distributed nationwide