State

Indiana product recalls

72,969 recalls have nationwide distribution and so reach Indiana. 9,556 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total: 9,556
Critical: 1,903
Severe: 2,136
Most recent: 2026-09-16

Of the 9,556 recalls naming Indiana we have scored against our rubric, 1,903 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,136 (22%) are Severe.

Which agencies issued them

These figures cover only the 9,556 recalls whose distribution notice names Indiana specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6176–6200 of 82525

HighUSDA FSIS·PHA-07302025-01·2025-07-30
Frozen Pork and Beef Tortellini Recalled for Undeclared Soy and Sesame Allergens
USDA FSIS issued a public health alert for frozen tortellini that may contain undeclared soy and sesame. Consumers with allergies should not consume the product.
Product
P.E. & F Inc. DBA DiMare's Specialty Foods — FSIS Issues Public Health Alert for Frozen Pork and Beef Tortellini Product Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
4 states
HighFDA (Food)·H-0312-2025·2025-07-30
Turkeyfoot Creek Creamery cookie dough ice cream has undeclared soy and wheat
Turkeyfoot Creek Creamery Cookie Dough Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy and wheat. All expiration dates are affected.
Product
Turkeyfoot Creek Creamery Cookie Dough Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lid
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-2147-2025·2025-07-30
EMPOWR dual mobility poly bearings were packaged with the wrong implant
EMPOWR Acetabular Dual Mobility Poly Bearings are being recalled because of a packaging discrepancy in which incorrect implants were packaged, discovered through a customer complaint. 20 units affected.
Product
Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD40 Model/Catalog Number: 952-28-40E Software Version: NA Product Description: The EMPOWR Dual Mobility" system is compatible with the EMPOWR Acetabular¿ system, 28mm femora
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-2135-2025·2025-07-30
HSG procedure trays label non-sterile iodine pouches as sterile
HSG Procedure Trays are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 171 units are affected.
Product
HSG Procedure Tray. Model Number: 6050T. The HSG Procedure Tray is for use in hysterosalpingography and sonohysterography procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2151-2025·2025-07-30
Nellcor bedside SpO2 monitor alarms may not be heard or recognized
The Covidien Nellcor Bedside SpO2 Patient Monitoring System is being recalled because alarms may not be heard or recognized, which the manufacturer links to treatment delay. 264,790 units are affected.
Product
Covidien Nellcor Bedside SpO2 Patient Monitoring System: REF: PM100N, 10005941, DLPM100N, DL10005941, DSPM100N, 10005941-SG, DS10005941, 10005941J, 10005941JP, 10005941JPN
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2148-2025·2025-07-30
EMPOWR dual mobility OD42 bearings were packaged with the wrong implant
EMPOWR Acetabular Dual Mobility Poly Bearings, catalog number 952-28-42F, are being recalled because of a packaging discrepancy in which incorrect implants were packaged. 20 units affected.
Product
Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD42 Model/Catalog Number: 952-28-42F Software Version: NA Product Description: The EMPOWR Dual Mobility" system is compatible with the EMPOWR Acetabular¿ system, 28mm femora
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-2165-2025·2025-07-30
Biofinity XR Toric contact lens blisters may have a leaking seal
Biofinity XR Toric Contact Lenses are being recalled because lens blisters may have an incomplete or leaking seal, which may render them unsterile. 397 units are affected.
Product
Biofinity XR Toric Contact Lens
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2168-2025·2025-07-30
SmartSync Patient Connector limited the window to abort high voltage therapy
The Medtronic CareLink SmartSync Patient Connector is being updated because in prior application versions the abort window during an induction test limited the user's ability to cancel high voltage therapy. 22,091 devices affected.
Product
Medtronic CareLink SmartSync Patient Connector, Model Number 24967 with the following software components: 1. Cobalt Crome application, Software Model Number D00U005; 2. Claria Amplia Compia application, Software Model Number D00U009; 3. Evera MRI application, Software M
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2130-2025·2025-07-30
SIGNA Architect gradient coils can produce acoustic noise above the limit
GE HealthCare SIGNA Architect MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.
Product
SIGNA Architect
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0536-2025·2025-07-30
Compounded quadruple ophthalmic solution returned subpotent assay results in stability testing
A compounded Tropicamide-Proparacaine-Phenylephrine-Ketorolac sterile ophthalmic solution is being recalled because of subpotent assay results during stability testing. 2,890 vials are affected.
Product
Tropicamide-Proparacaine-Phenylephrine-Ketorolac, Sterile Ophthalmic Solution, 1% 0.5% 2.5% 0.5%, 5mL, 2x5ML vial per carton, Rx Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-733-05.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0537-2025·2025-07-30
Clomipramine capsules failed a degradation product specification at expiry testing
Clomipramine Hydrochloride Capsules USP 25 mg are being recalled after an out of specification result for an unspecified degradation product during retention sample testing at expiry. 2,724 bottles affected.
Product
CLOMIPRAMINE HYDROCHLORIDE — CLOMIPRAMINE HYDROCHLORIDE (CLOMIPRAMINE HYDROCHLORIDE CAPSULES)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2163-2025·2025-07-30
ACUVUE OASYS MAX multifocal daily lenses have bubbles and voids
ACUVUE OASYS MAX 1-Day MULTIFOCAL contact lenses are being recalled because of defects, specifically bubbles and voids, identified during standard finished goods testing. 114,165 lenses affected.
Product
ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0327-2025·2025-07-30
Sushi wasabi mini packs do not declare Yellow 5 on label
Sushi Wasabi 5 gram ready to eat mini packs are being recalled because the individual consumer size label does not declare the ingredient Yellow 5. 1,848 cases are affected.
Product
Sushi Wasabi; 5 grams (Ready to eat) Ingredients: Horseradish, Corn Oil, Salt, Water, Citric Acid, Tumeric, FD&C Blue#1 Distributed by: Tokyo Nori U.S.A, City of Industry, CA 91746
Category
Food
Distribution
21 states
SevereNHTSA·25V495000·2025-07-29
Mack Recalls 2026 Granite Trucks Due to Brake Drum Incompatibility
Mack Trucks is recalling 2026 Granite GR trucks because incompatible brake drums and steer axles may cause loss of brake function, increasing crash risk.
Product
MACK — MACK GRANITE GR (4)
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25E046000·2025-07-29
Terran Industries Recalls 7000lb Axle Assemblies Due to Suspension Defect
Terran Industries is recalling 7000lb axle assemblies because incorrect suspension components may have been installed, posing a risk of axle spring failure or wheel detachment.
Product
SUSPENSION:MULTIPLE AXLE recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V494000·2025-07-28
Kia Telluride door belt molding trim can delaminate and detach
Kia is recalling certain 2023-2025 Telluride vehicles because the door belt molding trim can delaminate and detach from the vehicle, becoming a road hazard.
Product
KIA — KIA TELLURIDE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V493000·2025-07-28
Kia K5 rear window trim pieces may loosen and detach
Kia is recalling certain 2023-2025 K5 vehicles because the left and right rear window trim pieces may loosen and detach, becoming a road hazard for other vehicles.
Product
KIA — KIA K5
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V491000·2025-07-28
Grech motorhome awnings can extend unintentionally during transit
Grech Motors is recalling certain 2020-2025 Strada, Turismo and Terreno motorhomes because the retractable awning may extend unintentionally while the vehicle is moving.
Product
GRECH — GRECH TERRENO, STRADA, TURISMO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V492000·2025-07-28
Porsche Recalls 2024-2025 Macan 4 Electric for Air Bag Defect
Porsche is recalling 2024-2025 Macan 4 Electric vehicles because front seat air bags may be improperly secured, potentially preventing proper deployment during a crash.
Product
PORSCHE — PORSCHE MACAN 4 ELECTRIC
Category
Vehicle
Distribution
Distributed nationwide
ModerateNHTSA·25V490000·2025-07-28
2026 Tesla Model Y vehicles recalled for inoperable horn
Tesla is recalling certain 2026 Model Y vehicles because the horn ground wire ring terminal may be improperly secured, causing the horn to fail. An inoperable horn increases the risk of crashes.
Product
TESLA — TESLA MODEL Y
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-07272025-01·2025-07-27
USDA Alerts on Ham Salad Products with Recalled Breadcrumbs
USDA FSIS issued a public health alert for Reser's and Molly's Kitchen ham salad products containing breadcrumbs recalled for possible Listeria monocytogenes contamination.
Product
Reser's Fine Foods, Inc. — FSIS Issues Public Health Alert For Ready-To-Eat Ham Salad Products Containing FDA-Regulated Breadcrumbs That Have Been Recalled Due to Possible Listeria Monocytogenes Contamination
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·25V486000·2025-07-25
Forest River Recalls 2025-2026 Motorhomes Due to Fuel Line Fire Risk
Forest River is recalling 2025-2026 Sunseeker, Solera, and other motorhomes because fuel line connectors may detach, creating a fire hazard.
Product
FOREST RIVER — FOREST RIVER, EAST TO WEST SUNSEEKER, SOLERA, LEPRECHAUN, FREELANDER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V488000·2025-07-25
Ford electronic brake booster can fail losing power brake assist
Ford is recalling certain 2025 Lincoln Navigator, F-150, Expedition, Bronco and Ranger vehicles because the Electronic Brake Booster module may malfunction, causing a loss of power brake assist.
Product
FORD — FORD, LINCOLN BRONCO, RANGER, NAVIGATOR, EXPEDITION
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V487000·2025-07-25
Mercedes EQB battery bus bar screws can cause sudden power loss
Mercedes-Benz is recalling certain 2022-2023 EQB 300 and EQB 350 4MATIC vehicles because the high voltage battery bus bar may be secured with incorrect screws, causing a sudden loss of drive power.
Product
MERCEDES-BENZ — MERCEDES-BENZ EQB 300 4MATIC, EQB 350 4MATIC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25E047000·2025-07-25
Ford Recalls Bronco Upfit Kits Due to Rearview Camera Compatibility Issues
Ford is recalling specific Bronco Upfit kits because the rearview camera may not display an image, increasing crash risk. Dealers will replace the camera free of charge.
Product
BACK OVER PREVENTION: SENSING SYSTEM: CAMERA recall
Category
Vehicle
Distribution
Distributed nationwide