State

Indiana product recalls

73,597 recalls have nationwide distribution and so reach Indiana. 9,592 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total: 9,592
Critical: 1,908
Severe: 2,534
Most recent: 2026-10-24

Of the 9,592 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 9,592 recalls whose distribution notice names Indiana specifically. The 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29751–29775 of 83189

CriticalFDA (Food)·F-0115-2021·2020-11-18
Starwest Botanicals Recalls Organic Elderberry Due to Salmonella Risk
Starwest Botanicals is recalling organic elderberry because a customer test detected Salmonella. The product was distributed nationwide and to two Canadian customers.
Product
Elderberry Whole Organic; Sambucus Nigra; Origin: Croatia Distributed in boxes with plastic liners. Various sizes Bulk UPC 7 67963 07314 3, Item # 209290-00 Starwest Botanicals,Inc. 161 Main Street, Sacramento, CA 95838 Certified Organic
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0107-2021·2020-11-18
Meijer Strawberry and Pineapple Cup Recalled for Salmonella Risk
Meijer is recalling 1,300 units of Fresh from Meijer Strawberry/Pineapple Cups due to a potential risk of Salmonella. The product was sold in six states.
Product
FRESH FROM MEIJER GS STRAWBERRY/PINEAPPLE CUP 6 OZ, 6oz Clear plastic container, UPC 219711302291
Category
Food
Distribution
6 states
CriticalFDA (Food)·F-0098-2021·2020-11-18
Meijer Recalls Cantaloupe and Honeydew Slices Due to Salmonella Risk
Meijer is recalling 24oz containers of Fresh from Meijer Cantaloupe and Honeydew Slices due to a potential risk of Salmonella. The product was sold in six states.
Product
FRESH FROM MEIJER CANTALOUPE AND HONEYDEW SLICES, 24oz Clear plastic container, UPC 220219600079
Category
Food
Distribution
6 states
CriticalFDA (Food)·F-0103-2021·2020-11-18
Meijer Fruit Tray Recalled for Potential Salmonella Risk
Meijer is recalling Fresh From Meijer Fruit Trays due to a potential risk of Salmonella. The product was sold in six states between September 26 and October 5.
Product
FRESH FROM MEIJER FRUIT TRAY, 49oz Clear plastic container, UPC 219214610008
Category
Food
Distribution
6 states
CriticalFDA (Food)·F-0097-2021·2020-11-18
Meijer Cantaloupe Chunks Recalled for Potential Salmonella Risk
Meijer is recalling Fresh from Meijer Cantaloupe Chunks due to a potential risk of Salmonella. The products were sold in six states.
Product
FRESH FROM MEIJER CANTALOUPE CHUNKS LARGE BOWL, 32oz Clear plastic container, UPC 219323109721. FRESH FROM MEIJER CANTALOUPE CHUNKS SMALL BOWL, 16oz Clear plastic container, UPC 220196109725. FRESH FROM MEIJER CANTALOUPE CHUNKS KOSHER - LG, 32oz Clear plastic container, UPC…
Category
Food
Distribution
6 states
SevereFDA (Devices)·Z-0425-2021·2020-11-18
Puritan Bennett 980 Ventilator Recalled for Battery Overheating Risk
Covidien is recalling Puritan Bennett 980 ventilators due to battery overheating and thermal damage risks that could cause burns or smoke exposure.
Product
Puritan Bennett 980 (PB980) Ventilator Series - Product Usage: for use on patient population sizes from Neonatal (NICU) through Adult who require respiratory support or mechanical ventilation SKU: 980X1ENDIUU 980X1ENDIUU 980X3FRAIQC 980X3DEDRAC 980X3ENNISB 980X3NLDRAC…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0104-2021·2020-11-18
Meijer Fruit Frenzy Bowls Recalled for Potential Salmonella Risk
Meijer is recalling Fresh From Meijer Fruit Frenzy Bowls due to a potential risk of Salmonella. The recall affects 60,415 units sold in six states.
Product
FRESH FROM MEIJER FRUIT FRENZY BOWL LARGE BOWL, 40oz Clear plastic container, UPC 219210112216. FRESH FROM MEIJER FRUIT FRENZY SMALL BOWL, 16oz Clear plastic container, UPC 219601612646. FRESH FROM MEIJER FRUIT FRENZY MEDIUM BOWL, 32oz Clear plastic container, UPC…
Category
Food
Distribution
6 states
SevereNHTSA·20V714000·2020-11-18
Alfa Romeo Giulia Recall for Rear Brake Disc Fracture Risk
FCA US LLC is recalling 2020 Alfa Romeo Giulia vehicles because rear brake discs may fracture, potentially reducing braking performance and increasing crash risk.
Product
ALFA ROMEO — ALFA ROMEO GIULIA
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0105-2021·2020-11-18
Meijer Mixed Fruit Cup Recalled for Potential Salmonella Risk
Meijer is recalling Fresh From Meijer Mixed Fruit Cups due to a potential risk of Salmonella. The product was sold in six states.
Product
FRESH FROM MEIJER MIXED FRUIT CUP 6 OZ, 6oz Clear plastic container, UPC 219712601393. FRESH FROM MEIJER MIXED FRUIT CUP, 6oz Clear plastic container, UPC 220124913172. FRESH FROM MEIJER MIXED FRUIT CUP 6 OZ, 6oz Clear plastic container, (GAS STATIONS), UPC 219712601393 PLU…
Category
Food
Distribution
6 states
SevereFDA (Food)·F-0100-2021·2020-11-18
Meijer Melons and Berries Recalled for Potential Salmonella Risk
Meijer is recalling Fresh from Meijer Melons & Berries with Dip due to a potential risk of Salmonella. The product was sold in six states.
Product
FRESH FROM MEIJER MELONS & BERRIES WITH DIP, 22oz Clear plastic container, UPC 220452914490
Category
Food
Distribution
6 states
SevereFDA (Food)·F-0101-2021·2020-11-18
Meijer Recalls Mixed Melon Products Due to Salmonella Risk
Meijer is recalling specific mixed melon products sold in six states due to a potential risk of Salmonella.
Product
FRESH FROM MEIJER MIXED MELON SLICES, 24oz Clear plastic container, UPC 220220600075. FRESH FROM MEIJER MIXED MELON CHUNKS LARGE BOWL, 32oz Clear plastic container, UPC 219334109727. FRESH FROM MEIJER MIXED MELON CHUNKS SMALL BOWL, 16oz Clear plastic container, UPC…
Category
Food
Distribution
6 states
SevereFDA (Drugs)·D-0072-2021·2020-11-18
H & H Remedies Recalls White Liniment Due to CGMP Deviations
H & H Remedies, LLC is voluntarily recalling 365 bottles of White Liniment due to Current Good Manufacturing Practice (CGMP) deviations.
Product
White Liniment packaged in a) 1 oz; b) 4 oz.; and c) 6 oz bottles. Mfg & Sold by: H & H Remedies, LLC c/o David A. Cox, 1219 South Broadway, New Philadelphia, OH 44663
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·20V715000·2020-11-18
Keystone Outback trailers recalled for potential frame rail buckling defect
Keystone is recalling 2019–2021 Outback recreational trailers for inadequate frame rail support that may cause buckling and crash risk. Owners should contact 1-866-425-4369 for the free frame reinforcement repair.
Product
KEYSTONE — KEYSTONE OUTBACK
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0106-2021·2020-11-18
Meijer Fruit Palooza Recalled for Potential Salmonella Risk
Meijer is recalling Fresh from Meijer Fruit Palooza due to a potential risk of Salmonella. The product was sold in six states.
Product
FRESH FROM MEIJER FRUIT PALOOZA, 22oz Clear plastic container, UPC 220450514739
Category
Food
Distribution
6 states
SevereNHTSA·20V713000·2020-11-18
Lamborghini Recalls 2019-2020 Urus Vehicles Due to Fuel Line Fire Risk
Lamborghini is recalling 2,831 2019-2020 Urus vehicles because high engine temperatures may damage the fuel line connector, causing a leak and increasing fire risk.
Product
LAMBORGHINI — LAMBORGHINI URUS
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0099-2021·2020-11-18
Meijer Triple Treat & Melon Recalled for Potential Salmonella Risk
Meijer is recalling Fresh from Meijer Triple Treat & Melon due to a potential risk of Salmonella. The product was sold in six states.
Product
FRESH FROM MEIJER TRIPLE TREAT & MELON, 22oz Clear plastic container, UPC 220453514736
Category
Food
Distribution
6 states
SevereFDA (Devices)·Z-0431-2021·2020-11-18
Stryker Recalls Cranial Perforators Due to Potential Metal Fragment Risk
Stryker is recalling Zyphr Disposable Cranial Perforators because a crack in the inner bit could release metal fragments into the surgical site or cause delayed disengagement.
Product
Stryker Zyphr Disposable Cranial Perforator, Large 14/11 mm- is a sterile, single use cutting accessory intended for cutting an 11 mm diameter access hole through the cranium of adult patients. Catalog Number: 5100-060-001
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0076-2021·2020-11-18
Baxter Recalls Bupivacaine Injection Due to Particulate Matter
Baxter Healthcare is recalling specific lots of Bupivacaine Hydrochloride Injection due to the presence of black and transparent particles in the solution.
Product
Bupivacaine Hydrochloride in 8.25% Dextrose Injection, USP Spinal 0.75% (15 mg/2 mL) 10 x 2 mL single-dose ampules, Rx only, Manufactured for: Baxter Healthcare Corporation Deerfield, IL 60015 USA, Manufactured by: Baxter Pharmaceuticals India Private Ltd Ahmedabad 382213 India…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0439-2021·2020-11-18
Fresenius Liberty Select Cycler Software Recall for Inadequate Dialysis Risk
Fresenius Medical Care is recalling Liberty Select Cycler devices with software version 2.9.0 because a software error may cause the device to fail to recognize extra fluid, potentially leading to inadequate dialysis.
Product
Liberty Select Cycler Software Version 2.9.0 Model Number 180343 and RTLR180343
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0446-2021·2020-11-18
United Imaging uCT 550 CT Scanners Recalled for Timer Display Error
Shanghai United Imaging Healthcare is recalling five uCT 550 CT scanners because an incorrect delay timer display may expose operators to unnecessary radiation.
Product
Computed Tomography X-Ray System, Model uCT 550, Rx, CE, GTIN: 06971576831036 - Product Usage: ntended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes and indicated for the whole body…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0445-2021·2020-11-18
United Imaging uCT 530 CT Scanner Recalled for Incorrect Timer Display
Shanghai United Imaging Healthcare Co., Ltd. is recalling four uCT 530 CT scanners because an incorrect delay timer may display, potentially exposing operators to unnecessary radiation.
Product
Computed Tomography X-Ray System, Model uCT 530, Rx, CE, GTIN: 06971576831012 - Product Usage: ntended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes and indicated for the whole body…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0427-2021·2020-11-18
Boston Scientific AMS 700 MS Pump Recall for Activation Difficulties
Boston Scientific is recalling AMS 700 MS Pumps due to reports of difficulty activating the device to inflate cylinders.
Product
AMS 700 MS Pump with and without InhibiZone, sold as individual units and also pre-connected to AMS 700 cylinders. Inflatable Penile Prosthesis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0447-2021·2020-11-18
United Imaging uCT 760 CT Scanner Recalled for Timer Display Error
Shanghai United Imaging Healthcare is recalling five uCT 760 CT scanners because a display error may cause operators to receive unnecessary radiation exposure.
Product
Computed Tomography X-Ray System, Model uCT 760, Rx, CE, GTIN: 06971576831043 - Product Usage: ntended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes and indicated for the whole body…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0428-2021·2020-11-18
Quidel SARS Antigen Test Kits Recalled for False Positive Results
Quidel is recalling 8,628 SARS Antigen FIA test kits due to false positive results. The affected units were distributed to 24 U.S. states.
Product
QUIDEL Sofia SARS Antigen FIA IVD REF 20374
Category
Medical Device
Distribution
23 states
HighFDA (Devices)·Z-0448-2021·2020-11-18
United Imaging uMI 550 PET/CT System Recalled for Incorrect CT Scan Delay Timer
Shanghai United Imaging Healthcare is recalling nine uMI 550 PET/CT systems because an incorrect CT scan delay timer may display, potentially exposing operators to unnecessary radiation.
Product
Positron Emission Tomography and Computed Tomography System, Model uMI 550, Rx, CE, GTIN: 06971576832026 - Product Usage: intended to be operated by qualified healthcare professionals to assist in the detection, localization, diagnosis, staging, restaging, treatment planning…
Category
Medical Device
Distribution
Distributed nationwide