State

Indiana product recalls

73,741 recalls have nationwide distribution and so reach Indiana. 9,596 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total: 9,596
Critical: 1,908
Severe: 2,534
Most recent: 2026-10-28

Of the 9,596 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 9,596 recalls whose distribution notice names Indiana specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34276–34300 of 83337

HighFDA (Devices)·Z-0689-2020·2019-12-25
Teleflex Recalls Arrow EZ-IO Intraosseous Vascular Access System Needles
Teleflex Medical is recalling 526,000 Arrow EZ-IO Intraosseous Vascular Access System kits because safety caps may dislodge, risking needle stick injuries and sterility compromise.
Product
Arrow EZ-IO Intraosseous Vascular Access System 25mm Needle+Stabilizer Kit, Product Code 9001P-VC-005 - Product Usage: The Arrow EZ-IO Intraosseous Vascular Access System provides intraosseous access in the proximal humerus, proximal tibia, and distal tibia of adult and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0706-2020·2019-12-25
DeRoyal Warrior Recovery Knee Brace Recalled for Hinge Breakage Risk
DeRoyal Industries is recalling Warrior Recovery Knee Braces because the hinge may break, causing the brace to come apart.
Product
DeRoyal KNEE BRACE, WARRIOR RECOVERY: 1) REF KB9000-01 2) REF 11-450A-00 3) REF 1150UTPP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0688-2020·2019-12-25
Teleflex Recalls Arrow EZ-IO Intraosseous Vascular Access System Needles
Teleflex Medical is recalling 526,000 Arrow EZ-IO Intraosseous Vascular Access System kits because safety caps may dislodge, exposing needles and compromising sterility.
Product
Arrow EZ-IO Intraosseous Vascular Access System 15mm Needle+Stabilizer Kit, Product Code 9018P-VC-005 - Product Usage: The Arrow EZ-IO Intraosseous Vascular Access System provides intraosseous access in the proximal humerus, proximal tibia, and distal tibia of adult and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0401-2020·2019-12-25
Whole Foods Recalls Chicken Orange and Vegetable Meals for Listeria Risk
Whole Foods Market is recalling Family Meal Chicken Orange and Vegetable products due to possible contamination with Listeria monocytogenes.
Product
Family Meal Chicken Orange and Vegetable UPC 22849900000 sold packaged in stores, PLU 28499
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0383-2020·2019-12-25
Whole Foods Recalls Salmon Dinner with Mild Italian for Listeria Risk
Whole Foods Market is recalling Salmon Dinner with Mild Italian for 2 due to possible contamination with Listeria monocytogenes.
Product
Salmon Dinner with Mild Italian for 2 packaged in the store UPC 20451300000
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0354-2020·2019-12-25
Whole Foods Recalls Wedge Greek Salad for Listeria Risk
Whole Foods Market is recalling Wedge Greek Salad served on the salad bar due to possible contamination with Listeria monocytogenes.
Product
Wedge Greek Salad served on the salad bar
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0653-2020·2019-12-25
AuroMedics Recalls Gabapentin Capsules Due to Foreign Tablet Presence
AuroMedics Pharma LLC is recalling specific lots of Gabapentin Capsules because a Losartan/HCTZ tablet was found in the bottles.
Product
Gabapentin Capsules, USP 100 mg, Rx Only, Distributed by: Aurobindo Pharma USA, Inc. Dayton, NJ 08810, NDC 65682-198-99
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0382-2020·2019-12-25
Whole Foods Recalls Salmon Dinner with Lemon Herb for Listeria Risk
Whole Foods Market is recalling Salmon Dinner with Lemon Herb for 2 due to possible contamination with Listeria monocytogenes.
Product
Salmon Dinner with Lemon Herb for 2 packaged in the store UPC 20451100000
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0696-2020·2019-12-25
Smith & Nephew Recalls PROFIX Mallets Due to Tip Detachment Risk
Smith & Nephew is recalling 1,371 PROFIX Mallets because the poly tip may detach during surgery, potentially releasing particles into the surgical field.
Product
smith&nephew PROFIX Mallet, 750 GRAMS, REF 71512452 - Product Usage: The PROFIX Mallet is a reusable surgical instrument used to tap instruments or implants during knee or hip surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0337-2020·2019-12-25
Gold Standard Baking Recalls Croissants Due to Missing Allergen Labels
Gold Standard Baking is recalling Freshness Guaranteed Croissants because the packaging is missing ingredient and nutrition labels, including required allergen information for milk, wheat, and soy.
Product
Freshness Guaranteed Croissants in clear plastic 12oz clamshell, 12 clamshells per case, item number 7012
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0705-2020·2019-12-25
Bio-Signal Group Recalls HydroDot Wave Prep Cups Due to B. cepacia Contamination
Bio-Signal Group Corp. is recalling HydroDot Wave Prep single-use cups due to potential contamination with Burkholderia cepacia. The product is distributed in six US states.
Product
HydroDot brand: Wave Prep Single use cups, 8.5 gm (0.3 oz) 24/box-Product 1700-24 - Product Usage: An electroconductive cream for use with external electrodes to reduce the impedance of the contact between the electrode surface and the skin. The cream is not intended for use…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0690-2020·2019-12-25
Teleflex Recalls Arrow EZ-IO Intraosseous Vascular Access System Needles
Teleflex Medical is recalling 526,000 Arrow EZ-IO Intraosseous Vascular Access System kits because safety caps may dislodge, exposing needles and compromising sterility.
Product
Arrow EZ-IO Intraosseous Vascular Access System 45mm Needle+Stabilizer Kit, Product Code 9079P-VC-005 - Product Usage: The Arrow EZ-IO Intraosseous Vascular Access System provides intraosseous access in the proximal humerus, proximal tibia, and distal tibia of adult and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0356-2020·2019-12-25
Whole Foods Recalls Roasted Cauliflower Salad Bar Item for Listeria Risk
Whole Foods Market is recalling Caulilini, Roasted with Roasted Garlic, served on the salad bar, due to possible contamination with Listeria monocytogenes.
Product
Caulilini, Roasted with Roasted Garlic served on the salad bar
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0704-2020·2019-12-25
Bio-Signal Group Recalls HydroDot Wave Prep Electroconductive Cream
Bio-Signal Group Corp. is recalling HydroDot Wave Prep electroconductive cream due to potential contamination with Burkholderia cepacia.
Product
HydroDot brand: Wave Prep 4 oz. tubes-Product 1710-03. An electroconductive cream for use with external electrodes - Product Usage: An electroconductive cream for use with external electrodes to reduce the impedance of the contact between the electrode surface and the skin.…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0682-2020·2019-12-25
Polymer Technology Systems Recalls A1CNow+ Systems Due to Software Bug
Polymer Technology Systems is recalling A1CNow+ Systems because a software bug may display incorrect numerical values instead of expected symbols.
Product
A1CNow+ Systems (professional use product), Software Version Revision D, REF Numbers US: 3021, 3024; EU: 3037, 3038, 3057, 3058
Category
Medical Device
Distribution
18 states
ModerateFDA (Devices)·Z-0685-2020·2019-12-25
ReliOn FastA1C Test Recalled for Software Bug Affecting Result Display
Polymer Technology Systems is recalling ReliOn FastA1C Tests due to a software bug that may display incorrect numerical values instead of expected symbols.
Product
ReliOn FastA1C Test, Software Version Revision D, REF Number 3055
Category
Medical Device
Distribution
18 states
ModerateFDA (Drugs)·D-0629-2020·2019-12-25
Lupin Recalls Memantine Hydrochloride Capsules Due to Dissolution Failure
Lupin Pharmaceuticals is recalling 3,726 bottles of Memantine Hydrochloride Extended-release Capsules because stability studies showed high out-of-specification dissolution results.
Product
MEMANTINE HYDROCHLORIDE — MEMANTINE HYDROCHLORIDE (MEMANTINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0709-2020·2019-12-25
Angiodynamics Recalls OARTRAC Prostate Balloon Kits Due to Accuracy Issues
Angiodynamics, Inc. is recalling 160 OARTRAC Prostate Immobilization Endorectal Balloon Device Kits because they may produce readings outside the expected accuracy range.
Product
OARTRAC PROSTATE IMMOBILIZATION ENDORECTAL BALLOON DEVICE KIT, Catalog Number: ORB-60F - Product Usage: pre-calibrated PSD sensors are intended for use during cancer treatments to measure photon and electron radiation therapy as an adjunct to treatment planning permitting…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0711-2020·2019-12-25
Angiodynamics Recalls MICRO-PSD Electron Sensors Due to Accuracy Concerns
Angiodynamics, Inc. is recalling 36 units of MICRO-PSD Electron sensors because they may provide readings outside the expected accuracy range.
Product
MICRO-PSD Electron, Catalog Number: PSD-EE5N - Product Usage: pre-calibrated PSD sensors are intended for use during cancer treatments to measure photon and electron radiation therapy as an adjunct to treatment planning permitting measurement and validation of radiation dose…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0684-2020·2019-12-25
Polymer Technology Systems Recalls Walgreens At-Home A1C Test Kits
Polymer Technology Systems is recalling 15,118 Walgreens At-Home A1C Test Kits due to a software bug that may display incorrect numerical values for extreme results.
Product
Walgreens At-Home A1C Test Kit, Software Version Revision D, REF Number 3056
Category
Medical Device
Distribution
18 states
ModerateFDA (Devices)·Z-0686-2020·2019-12-25
CVS Health At Home A1C Test Kit Recalled for Software Bug
Polymer Technology Systems is recalling CVS Health At Home A1C Test Kits due to a software bug that may display incorrect numerical values for extreme results.
Product
CVS Health At Home A1C Test Kit, Software Version Revision D, REF Number 3059
Category
Medical Device
Distribution
18 states
ModerateFDA (Devices)·Z-0703-2020·2019-12-25
Teleflex Sheridan Endobronchial Tubes Recalled for Incorrect Labeling
Teleflex Medical is recalling Sheridan Endobronchial Tubes due to incorrectly labeled tracheal and bronchial swivel connectors.
Product
HUDSON RCI SHERIDAN SHERI-BRONCH Endobronchial Tube REF 5-16135 - Product Usage: The Sheridan Endobronchial Tubes are intended for use in Thoracic surgery, brochospirometry, adminitration of endobronchial anesthesia and other uses commonly requiring endobronchial intubation. The…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0691-2020·2019-12-25
Integra Recalls Mislabeled Ascension Silicone PIP Joint Implants
Integra Lifesciences is recalling nine Ascension Silicone PIP implants that were mislabeled as size 1 but contained size 0 implants.
Product
Ascension¿ Silicone PIP-Silicone PIP Sz 1, Model Number: SPIP5201WW - Product Usage: The Ascension Silicone PIP implant is intended for cementless replacement of the proximal interphalangeal joint in patients with advanced osteoarthritis, post-traumatic arthritis and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0713-2020·2019-12-25
Angiodynamics Recalls Micro-PSD External Beam Photon Sensors
Angiodynamics, Inc. is recalling 48 Micro-PSD External Beam Photon sensors due to potential accuracy issues. The devices are used to measure radiation therapy during cancer treatment.
Product
MICRO-PSD EXTERNAL BEAM PHOTON, Catalog Number: PSD-PE5N - Product Usage: pre-calibrated PSD sensors are intended for use during cancer treatments to measure photon and electron radiation therapy as an adjunct to treatment planning permitting measurement and validation of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0683-2020·2019-12-25
Polymer Technology Systems Recalls A1CNow SELF CHECK Software Bug
Polymer Technology Systems is recalling A1CNow SELF CHECK devices due to a software bug that may display incorrect numerical values instead of expected symbols.
Product
A1CNow SELF CHECK (European), Software Version Revision D, REF Numbers 3054, 3062
Category
Medical Device
Distribution
18 states