State

Indiana product recalls

72,992 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 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9251–9275 of 82548

SevereFDA (Devices)·Z-0296-2025·2024-11-20
Philips LifeVent EVO2 ventilators recalled for potential sensor accuracy failure
Philips Respironics is recalling LifeVent EVO2 ventilators due to potential aerosol deposit accumulation on the internal flow sensor that could cause inaccurate measurements during ventilation.
Product
LifeVent EVO2. Model Number: SP2100X26B. Intended for invasive and non-invasive ventilation of pediatric through adult patients weighing at least 2.5 kg in institutional, home, and non-emergency transport settings.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0293-2025·2024-11-20
Trilogy EV300 ventilator: potential flow sensor malfunction from aerosol accumulation
Philips Respironics is recalling 34,146 Trilogy EV300 ventilators due to potential aerosol accumulation on the internal flow sensor, which could cause inaccurate ventilation measurements.
Product
Trilogy EV300. Model Numbers: DS2200X11B, IN2200X15B, BL2200X15B, BR2200X18B, CA2200X12B, DE2200X13B, GB2200X15B, ND2200X15B, ES2200X15B, FR2200X14B, FX2200X15B, EU2200X15B, IA2200X15B, IT2200X21B, KR2200X15B, TR2200X15B, EE2200X15B. Intended for invasive and non-invasive venti
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0295-2025·2024-11-20
Ventilator Model LD2110X23B Recalled for Potential Sensor Measurement Failure
Philips Respironics is recalling 1,322 Garbin Evo ventilators (Model LD2110X23B) worldwide due to potential aerosol accumulation that could cause inaccurate flow sensor readings, posing a risk to patient care.
Product
Garbin Evo. Model Number: LD2110X23B. Intended for invasive and non-invasive ventilation of pediatric through adult patients weighing at least 2.5 kg in institutional, home, and non-emergency transport settings.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0305-2025·2024-11-20
Anesthesia workstation piston ventilator may fail before or during use
Draeger Medical is recalling Atlan A350XL anesthesia workstations due to potential piston ventilator failure that may occur before use or during mechanical ventilation.
Product
Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Component: Not applicable
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24V877000·2024-11-20
Hyundai Tucson console wiring may allow shifting out of Park unbraked
Hyundai is recalling certain 2025 Tucson and Santa Cruz vehicles because misrouted console wiring may allow the transmission to shift out of Park without the brake applied.
Product
HYUNDAI — HYUNDAI SANTA CRUZ, TUCSON
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0290-2025·2024-11-20
Trilogy Evo O2 Ventilators Recalled for Potential Flow Sensor Malfunction
Philips Respironics recalled 24,249 Trilogy Evo O2 ventilators because in-line nebulizer configurations may allow aerosol deposits to accumulate on the device's flow sensor, potentially causing inaccurate flow measurements.
Product
Trilogy Evo O2. Model Numbers: FP2100X10, DS2100X11B, IN2100X15B, DE2100X13B, IA2100X15B, EU2100X15B, LA2100X15B, EE2100X15B, FX2100X15B, ES2100X15B, ND2100X15B, FR2100X14B, IT2100X21B, JP2100X16B, IN2100X19, EU2100X19. Intended for invasive and non-invasive ventilation of pedi
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0291-2025·2024-11-20
Philips Trilogy Evo ventilators recall: flow sensor fouling risk
Philips Respironics is recalling Trilogy Evo ventilators due to potential aerosol deposits on the internal flow sensor, which could cause inaccurate flow measurements during ventilation.
Product
Trilogy Evo. Model Numbers: DS2110X11B, UDS2110X11B, RDS2110X11B, CA2110X12B, JP2110X16B, IN2110X15B, DE2110X13B, AU2110X15B, BL2110X15B, EU2110X15B, BR2110X18B, LA2110X15B, EE2110X15B, FR2110X14B, GB2110X15B, ND2110X15B, ES2110X15B, IA2110X15B, IT2110X21B, KR2110X15B, TR2110X15B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0387-2025·2024-11-20
Halyard Open Heart Surgical Kits Recalled for Loose Metal Flakes in Instruments
AVID Medical is recalling Halyard Open Heart Pack Main surgical kits because sponge forceps and towel clamps may contain loose metal flakes that could detach and enter a patient's surgical site.
Product
Halyard OPEN HEART PACK MAIN - Medical convenience kits Model Number: ESJH003-02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0436-2025·2024-11-20
AVID Medical Recalls Halyard GYN PAC Kits Due to Metal Flakes
AVID Medical is recalling Halyard GYN PAC medical convenience kits because sponge forceps and towel clamps may release metal flakes that could enter a patient's surgical site.
Product
Halyard GYN PAC - Medical convenience kits Model Number: SJGY20-02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0331-2025·2024-11-20
VYGON 250 mL IV Fluid Containers Recalled for Leaks During Filling
The Metrix Company is recalling VYGON 250 mL IV fluid containers that have been found to leak during filling. Leaking containers cannot properly contain intravenous fluid.
Product
VYGON 250 mL EMPTY EVA CONTAINER With 2 Ports, REF CMS-9602; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0400-2025·2024-11-20
Surgical procedure kits recalled due to loose metal flakes in instruments
AVID Medical is recalling Halyard BASIC PROCEDURE PACK surgical instrument kits because sponge forceps and towel clamps may contain loose metal flakes that could enter a patient's surgical site and cause local or foreign body reactions.
Product
Halyard BASIC PROCEDURE PACK - Medical convenience kits Model Number: GRAN019-06
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0443-2025·2024-11-20
Halyard Pacemaker Drape Surgical Instruments Recalled for Loose Metal Flakes
AVID Medical recalls Halyard Pacemaker Drape surgical instruments because metal flakes may detach from sponge forceps and towel clamps. Loose metal fragments could enter surgical sites undetected and cause local or foreign body reactions.
Product
Halyard PACEMAKER DRAPE - Medical convenience kits Model Number: VAST020-06
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0347-2025·2024-11-20
Approach Hydro ST Micro Wire Guide Recalled for Incorrect Expiration Dates
Cook Incorporated is recalling Approach Hydro ST Micro Wire Guide devices because affected device labels contain incorrect expiration dates. Using mislabeled devices beyond their actual expiration creates a risk of device failure and patient harm.
Product
Approach Hydro ST Micro Wire Guide; Catalog prefix HMW Reference Part Numbers: HMW-14-135-ST HMW-14-190-ST HMW-14-300-ST
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0464-2025·2024-11-20
IMMULITE 2000 PSA assay does not meet high-dose analytical performance claim
Siemens Healthcare is recalling certain IMMULITE 2000 PSA assay diagnostic kits because they do not perform as claimed for high-concentration samples used on IMMULITE 2000 analyzers.
Product
IMMULITE 2000 PSA assay, Catalog Number L2KPTS2(D) (SMN 10706281) and Catalog Number L2KPTS6(D) (SMN 10706282)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0393-2025·2024-11-20
Halyard Anterior Hip Pack surgical kits recalled due to loose metal flakes
AVID Medical is recalling Halyard Anterior Hip Pack surgical kits because sponge forceps and towel clamps may have loose metal flakes that could detach, enter a patient's surgical site undetected, and cause local or foreign body reactions.
Product
Halyard ANTERIOR HIP PACK - Medical convenience kits Model Number: EUOR001-06
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0434-2025·2024-11-20
Surgical instrument kits recalled for loose metal flakes
AVID Medical is recalling Halyard CPT EP PACK surgical convenience kits due to loose metal flakes on forceps and towel clamps. Detached metal flakes could enter surgical sites and potentially cause local tissue reactions or foreign body complications.
Product
Halyard CPT EP PACK - Medical convenience kits Model Number: SHAN442-04
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0392-2025·2024-11-20
Halyard cardiac surgical kit recalled for loose metal flakes risk
AVID Medical is recalling Halyard cardiac surgical kits (Model ESJH017-03) due to sponge forceps and towel clamps that may shed small metal flakes during surgery. These metal flakes could enter the patient's surgical site, potentially causing local or foreign body reactions.
Product
Halyard KIT, CARDIAC ROBOTIC - Medical convenience kits Model Number: ESJH017-03
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0349-2025·2024-11-20
Surgical hip procedure kit recalled for incomplete product seals
Medline is recalling CARROLLTON HIP FX surgical kits due to incomplete seals on items within the kit. Affected units contain Lot Number 24EBP466 and were distributed in Tennessee.
Product
CARROLLTON HIP FX Convenience kit used for surgical procedures, SKU SYNJ910003A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0337-2025·2024-11-20
IV Fluid Pouches Found to Leak During Filling
The Metrix Company is recalling SECURE 50 mL EVA containers used for intravenous fluid administration because a limited number of pouches have been found to leak during filling. Affected products were distributed nationwide and to Canada.
Product
SECURE 50 mL EMPTY EVA CONTAINER With 2 Ports, REF 66042; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0405-2025·2024-11-20
Halyard GYN TRAY surgical kits recalled for loose metal flakes
AVID Medical is recalling 136 units of Halyard GYN TRAY surgical kits due to small loose metal flakes that could detach from sponge forceps and towel clamps. These metal fragments could enter a patient's surgical site undetected, causing local or foreign body reactions.
Product
Halyard GYN TRAY - Medical convenience kits Model Number: LANC014-19
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0397-2025·2024-11-20
Halyard surgical kit recalled for loose metal flakes in forceps and clamps
AVID Medical is recalling Halyard KIT, SPINE surgical convenience kits due to loose metal flakes on sponge forceps and towel clamps. The flakes could detach and enter a patient's surgical site, potentially causing local or foreign body reactions.
Product
Halyard KIT, SPINE - Medical convenience kits Model Number: EUOR004-03
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0419-2025·2024-11-20
Halyard Lower Extremity Pack surgical kits recalled for loose metal fragments
AVID Medical is recalling Halyard Lower Extremity Pack surgical kits because sponge forceps and towel clamps may shed loose metal flakes that could enter a patient's surgical site undetected, potentially causing local or foreign body reactions.
Product
Halyard LOWER EXTREMITY PACK - Medical convenience kits Model Number: PANJ001-03
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0044-2025·2024-11-20
Lanthanum Carbonate Chewable Tablets Recalled for Crushed and Broken Tablets
Cipla USA is recalling Lanthanum Carbonate Chewable Tablets (1000mg) distributed nationwide due to complaints of crushed and broken tablets that fail manufacturing specifications.
Product
Lanthanum Carbonate Chewable Tablets, 1000mg, 10-count bottle, Rx only, Manufactured for Exelan Pharmaceuticals, NDC 76282-0478-90
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0334-2025·2024-11-20
IV Bag Containers Recalled for Leaking During Filling Process
The Metrix Company is recalling CORMIX 500 mL IV bag containers that may leak during the filling process. These plastic pouches are intended for intravenous fluid administration.
Product
CORMIX 500 mL EMPTY EVA CONTAINER With 2 Ports, REF MS64050; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0426-2025·2024-11-20
Surgical Kit Components Recalled for Potential Metal Fragment Detachment
AVID Medical is recalling Halyard ORAL SURGERY HEAD medical convenience kits (Model SAMM029-15) due to potential loose metal flakes that could detach from forceps and clamps and enter the surgical site, posing risk of local or foreign body reactions.
Product
Halyard ORAL SURGERY HEAD - Medical convenience kits Model Number: SAMM029-15
Category
Medical Device
Distribution
Distributed nationwide