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.

41751–41775 of 83407

SevereFDA (Drugs)·D-1109-2018·2018-08-29
A-S Medication Solutions Recalls Valsartan Tablets Due to Carcinogen Impurity
A-S Medication Solutions LLC is recalling 178 bottles of Valsartan Tablets, 80 MG, because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Product
Valsartan Tablets, 80 MG, 30-count bottle (NDC 54569-6582-0, 90-count bottle (NDC 54569-6582-1), Rx Only, MFG: Zhejiang Huahai Pharma, Linhai, Zhejiang 317024 China
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1115-2018·2018-08-29
Hetero Labs Recalls Valsartan Tablets Due to Carcinogen Impurity
Hetero Labs Limited is recalling Valsartan tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Product
VALSARTAN — VALSARTAN (VALSARTAN)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1116-2018·2018-08-29
Hetero Labs Recalls Valsartan Tablets Due to Carcinogen Impurity
Hetero Labs is recalling Valsartan tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Product
VALSARTAN — VALSARTAN (VALSARTAN)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2753-2018·2018-08-29
Handicare P600 Series Patient Lift Recalled for Strap Wear and Breakage
Handicare USA Inc. is recalling four P600 Series patient lifts due to premature strap wear and breakage at maximum weight conditions.
Product
Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2860-2018·2018-08-29
Philips DigitalDiagnost Footplate Hook Recall for Injury Risk
Philips is recalling DigitalDiagnost Rel.4 Upgrades because a defective hook may allow the footplate to fall or swing, potentially injuring patients or operators.
Product
DigitalDiagnost Rel.4 Upgrades (Stitching Patient Support) 712084
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·18V571000·2018-08-29
Entegra Odyssey Recall: Damaged Hydraulic Hoses May Cause Fire
Entegra Coach is recalling 2018 Odyssey vehicles because damaged leveling system hydraulic hoses may leak fluid onto the exhaust system, increasing the risk of a fire.
Product
ENTEGRA — ENTEGRA redundant ODYSSEY
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2844-2018·2018-08-29
Philips DigitalDiagnost Release 3 Footplate Hook Recall
Philips is recalling DigitalDiagnost Release 3 units because a defective hook may allow the footplate to fall or swing, posing a risk of injury to patients or operators.
Product
DigitalDiagnost Release 3 (Stitching Patient Support) 712025
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1113-2018·2018-08-29
Hetero Labs Recalls Valsartan Tablets Due to Carcinogen Impurity
Hetero Labs Limited is recalling Valsartan tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Product
VALSARTAN — VALSARTAN (VALSARTAN)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1114-2018·2018-08-29
Hetero Labs Recalls Valsartan Tablets Due to Carcinogen Impurity
Hetero Labs Limited is recalling Valsartan tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Product
VALSARTAN — VALSARTAN (VALSARTAN)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2741-2018·2018-08-29
Compass Health Brands Recalls CPAP Mask Cushions Due to Design Incompatibility
Compass Health Brands is recalling CPAP mask cushions because a design change makes them incompatible with previous elbow parts, potentially causing unacceptable CO2 porting.
Product
CPAP Mask Cushion, Model Nos. PB781S, PB781M, PB781L, 781S, 781M and 781L Product Usage: A CPAP mask is attached to an end user s face and a CPAP machine, to treat end users with sleep apnea. The replacement cushion is a non-durable component that requires replacement every…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1837-2018·2018-08-29
Graeter's Key Lime Pie Ice Cream Recalled for Wheat Mislabeling
Graeter's is recalling 4,056 pints of Key Lime Pie ice cream because it is labeled gluten-free but contains wheat.
Product
Graeter's HANDCRAFTED French Pot ICE CREAM, Limited Edition KEY LIME PIE**ONE PINT (473 ml)**Nutrition Facts**GLUTEN FREE**INGREDIENTS: CREAM, MILK, CANE SUGAR, GRAHAM PIE PIECES, WHEAT FLOUR**CONTAINS:MILK, EGG, WHEAT,& SOY**Manufactured by: Graeter's Ice Cream, Cincinnati…
Category
Food
Distribution
15 states
HighFDA (Devices)·Z-2842-2018·2018-08-29
Philips DigitalDiagnost 4 Flex Footplate Recall Due to Injury Risk
Philips is recalling two DigitalDiagnost 4 Flex units because a defective hook allows the footplate to fall, posing an injury risk to patients or operators.
Product
DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2861-2018·2018-08-29
Philips DigitalDiagnost Release 3 Footplate Hook Recall for Injury Risk
Philips is recalling DigitalDiagnost Release 3 units because a defective hook may allow the footplate to fall or swing, posing an injury risk to patients or operators.
Product
DigitalDiagnost Release 3 (Stitching Patient Support) 712025
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1833-2018·2018-08-29
Dole Classic Coleslaw Recalled for Potential Metal Fragments
Dole Fresh Vegetables is recalling a limited quantity of Classic Coleslaw due to the potential for metal fragments in the product.
Product
Dole Classic Coleslaw, 14 oz. (397 g) plastic bag; Green Cabbage, shredded carrots. UPC Code 7143001066 Distributed by Dole Fresh Vegetables, Inc., Monterey, CA Case - 10.5 lbs - 12-14 oz. bags. (01) 20071430010666; (10) 2012006212W 8653
Category
Food
Distribution
13 states
HighFDA (Devices)·Z-2850-2018·2018-08-29
Philips DigitalDiagnost 4 Flex Footplate Recall for Injury Risk
Philips is recalling DigitalDiagnost 4 Flex and Value units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Product
DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2847-2018·2018-08-29
Philips CombiDiagnost R90 Footplate Hook Recall for Injury Risk
Philips is recalling CombiDiagnost R90 units because a defective hook may allow the footplate to fall, posing an injury risk to patients or operators.
Product
CombiDiagnost R90 (Stitching Patient Support) 709030
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2849-2018·2018-08-29
Philips DigitalDiagnost 4 Chest Footplate Recall Due to Injury Risk
Philips is recalling DigitalDiagnost 4 Chest units because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Product
DigitalDiagnost 4 Chest / Emergency (Stitching Patient Support) 712029
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2869-2018·2018-08-29
BD BBL GC-Lect Agar Recalled Due to Incorrect Antibiotic Ingredient
Becton Dickinson is recalling BD BBL GC-Lect Agar plates because some were made with Gentamicin instead of Vancomycin, which may cause false negative gonorrhea test results.
Product
BD BBL GC-Lect Agar; Cat. No. 297715 The device is a selective medium providing enhanced growth and recovery of Neisseria gonorrhoeae and better inhibition of contamination bacteria and fungi.
Category
Medical Device
Distribution
29 states
HighFDA (Devices)·Z-2873-2018·2018-08-29
GE Healthcare Optima CT660 Systems Recalled for Damaged Cable Hazard
GE Healthcare is recalling Optima CT660 systems because a damaged cable may expose 120VAC to service engineers working inside the gantry.
Product
GE Healthcare Optima CT660. The systems are intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications. Sold only outside the U.S. under the following product names: CT OPTIMA 660, CT OPTIMA 660 LONG BJG SKD RUS, CT OPTIMA 660 LONG BJG SKD…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2840-2018·2018-08-29
Elekta Digital Accelerator Recall for Potential Uncontrolled Detector Arm Extension
Elekta is recalling 2,998 Digital Accelerators worldwide due to a potential for uncontrolled extension of iViewGT or XVI detector arms.
Product
ELEKTA Digital Accelerator under the following brand names: Elekta Synergy, Synergy S, Synergy Platform, Precise Digital Accelerator, Infinity, Axesse, and Versa HD
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·18763·2018-08-29
BSN Sports Recalls Rubber Critter Toys for Lead Paint Violation
BSN Sports is recalling rubber critter toys because the orange and yellow paint contains lead levels exceeding federal bans. No injuries have been reported.
Product
Rubber critter toys
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2858-2018·2018-08-29
Philips DigitalDiagnost Dual Detector Footplate Recall for Injury Risk
Philips is recalling DigitalDiagnost Dual Detector units because the footplate hook may fail, causing the plate to fall and injure patients or operators.
Product
DigitalDiagnost Dual Detector (Stitching Patient Support) 712022
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2854-2018·2018-08-29
Philips DigitalDiagnost 4.1 Flex Footplate Recall for Injury Risk
Philips is recalling DigitalDiagnost 4.1 Flex and Value units because the footplate hook may fail, causing the footplate to fall and injure patients or operators.
Product
DigitalDiagnost 4.1 Flex / Value (Stitching Patient Support) 712028
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2870-2018·2018-08-29
GE Healthcare Recalls CT Systems Due to Damaged Cable Electrical Hazard
GE Healthcare is recalling specific CT systems because a damaged cable may expose 120VAC to service engineers working inside the gantry.
Product
GE Healthcare Revolution EVO, Optima CT660, Optima CT670, Optima CT680. The systems are intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications. Sold under the following product names: CT GOLDSEAL LIGHTSPEED ULTRA, CT OPTIMA 660, CT OPTIMA…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2864-2018·2018-08-29
Philips DigitalDiagnost Upgrades Recalled Due to Footplate Safety Hazard
Philips is recalling DigitalDiagnost Upgrades because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Product
DigitalDiagnost Upgrades (Stitching Patient Support) 712083
Category
Medical Device
Distribution
Distributed nationwide