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.

42551–42575 of 83407

SevereFDA (Food)·F-1598-2018·2018-07-04
Utz and Weis Tortilla Chips Recalled for Undeclared Milk Allergen
Utz Quality Foods is voluntarily recalling select tortilla chip products due to potential contamination with undeclared milk allergen.
Product
Utz Restaurant Style Tortilla Chips; Net Wt 17 oz; White Corn Tortilla Chips; UPC: 0-41780-00383-6; Exp. Date Jun 16 18; UTZ Quality Foods, Inc., Hanover, PA 17331; Utz Restaurant Style Tortilla Chips; Net Wt 11.5 oz; White Corn Tortilla Chips; UPC: 0-41780-00384-3; Exp…
Category
Food
Distribution
32 states
SevereFDA (Food)·F-1602-2018·2018-07-04
Utz Recalls Golden Flake Tortilla Chips for Undeclared Milk Allergen
Utz Quality Foods is voluntarily recalling select Golden Flake tortilla chips due to potential contamination with undeclared milk allergen.
Product
Golden Flake TORTIYAHS! Superior Dipping Chips; Net Wt 12.5 oz Tortilla Chips; Golden Flake Snack Foods, Inc. Birmingham, AL 35201; UPC: 0-72080-41000-0; Exp date: JUN 2 18 to JUN 23 18;
Category
Food
Distribution
32 states
SevereFDA (Food)·F-1601-2018·2018-07-04
Utz Recalls Tortilla Chips Due to Undeclared Milk Allergen
Utz Quality Foods is voluntarily recalling select tortilla chip items due to potential contamination with undeclared milk allergen.
Product
Weis Signature Collection No Salt Added White Corn Tortilla Chips; Net Wt 11 oz; Manufactured For Weis Markets, Sunbury, PA 17801; UPC: 0-41497-00427-0; Exp date: May 26 18 to JUN 16 18;
Category
Food
Distribution
32 states
SevereFDA (Devices)·Z-2300-2018·2018-07-04
Philips OmniDiagnost-Eleva X-ray System Recalled Due to Table Rotation Hazard
Philips is recalling 508 OmniDiagnost-Eleva X-ray systems because a broken actuator fixation can cause the table to rotate uncontrollably, posing a risk of injury.
Product
OmniDiagnost-Eleva X-ray system Angiographic and Diagnostic, Product Nos. 708026, 708027, 708028
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2323-2018·2018-07-04
St Jude Medical Recalls Promote Quadra ICDs for Security Firmware Update
St Jude Medical is recalling Promote Quadra implantable cardiac devices to release new firmware that strengthens security against unauthorized access.
Product
Promote Quadra, Sterile EO, Model # / Part #: CD3221-36/100025054, 60019195; CD3223-36P/100013763; CD3239-40/100029115, 100029254, 100037181; CD3239-40Q/100029116, 100029244, 100037115
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2320-2018·2018-07-04
St Jude Medical Recalls Fortify ICDs and CRT-Ds for Security Firmware Update
St Jude Medical is recalling Fortify ICDs and CRT-Ds to release new firmware that strengthens security against unauthorized access. Older devices may require permanent disabling of RF communication.
Product
Fortify, Sterile EO, Model #/ Part #: CD1231-40/100029238,100030095, 100041981; CD1231-40Q/100029229, 100030087, 100041982; CD1233-40/100029230, 100029250, 100029259,100031058, 100059778, 100070017; CD1233-40Q/100029260, 100029271, 100029277, 100031104, 100070089…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2287-2018·2018-07-04
Teleflex Universal Shears Recalled Due to Handle Melting During Sterilization
Teleflex Medical Europe Ltd is recalling 573 units of Pilling Universal Shears because incorrect plastic was used for the handles, causing them to melt during sterilization.
Product
Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2", REF 142542 Product Usage: general surgical scissors
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2317-2018·2018-07-04
Medtronic Model 53401 Pacemakers Recalled for Unexpected Power Reset
Medtronic is recalling 1,108 Model 53401 temporary external pacemakers because they may revert to nominal settings during use due to an unexpected power on reset.
Product
Single Chamber Temporary External Pacemaker, Model 53401
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-2313-2018·2018-07-04
Siemens Artis zee MP Recall for Display Failure After Power Save
Siemens is recalling Artis zee MP systems because the display may fail to show an image after power save mode, potentially requiring procedure cancellation or patient transfer.
Product
Artis zee MP, Material no. 10094139, for angiography and whole body radiographic/fluoroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2322-2018·2018-07-04
St Jude Medical Recalls High Voltage Implantable Cardiac Devices for Security Firmware
St Jude Medical is releasing new firmware for high voltage implantable cardiac devices to strengthen security against unauthorized access.
Product
Promote, Sterile EO, Model #/ Part #: 3207-30/60010740-207, 60010740-407; 3207-36/60010743-207, 60010743-407; 3213-36/50022126-001, 60013879-307, 60013879-407, 60013879-707; CD3211-36/100006984,100012548, 100012550, 100016680, 100031621, 100035618, 100035619, 100042487…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2280-2018·2018-07-04
Randox Liquid Assayed Specific Protein Control Recalled for Stability Issues
Randox Laboratories is recalling Liquid Assayed Specific Protein Control - Level 3 because Free Kappa light chains increase over shelf life, potentially delaying diagnostic results.
Product
Randox Liquid Assayed Specific Protein Control - Level 3 (SP Control 3), Cat. no. PS2684
Category
Medical Device
Distribution
6 states
HighFDA (Devices)·Z-2305-2018·2018-07-04
Siemens Artis Q.zen Biplane Recalled for Display Failure
Siemens Medical Solutions is recalling two Artis Q.zen biplane systems because the display may fail to show images after power save mode, potentially requiring treatment cancellation or patient transfer.
Product
Artis Q.zen biplane, Material no. 10848355, for angiography and whole body radiographic/fluoroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2304-2018·2018-07-04
Siemens Artis Q Ceiling Recalled for Display Failure After Power Save
Siemens Medical Solutions is recalling five Artis Q ceiling units because the display may fail to show an image after exiting power save mode, potentially requiring treatment cancellation.
Product
Artis Q ceiling, Material no. 10848281, for angiography and whole body radiographic/fluoroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2314-2018·2018-07-04
Siemens Artis zeego X-ray System Recalled for Display Failure
Siemens Medical Solutions is recalling 56 Artis zeego systems because the display may fail to show images after power save mode, potentially requiring procedure cancellation.
Product
Artis zeego, Material no. 10280959 , for angiography and whole body radiographic/fluoroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2308-2018·2018-07-04
Siemens Artis zee Biplane Recalled for Display Failure After Power Save
Siemens is recalling 68 Artis zee biplane systems because the large display may remain black after exiting power save mode, potentially requiring treatment cancellation or patient transfer.
Product
Artis zee biplane, Material no. 10094141, for angiography and whole body radiographic/fluoroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2288-2018·2018-07-04
HLD Systems Washer Pasteurizer Recalled for Terminal Block Overheating
Cenorin, LLC is recalling 14 HLD Systems 600 Series Washer/Pasteurizers because a supplier quality issue with terminal blocks may cause overheating, charring, or burning.
Product
HLD Systems 600 Series Washer/Pasteurizer, UDI (01) 0085249007009 (11) 160929 (21) 61160; Model 610HT, 115V & Model 610HT, 230V Product Usage: Clean and thermally disinfect medical devices using full immersion pasteurization
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2327-2018·2018-07-04
St Jude Medical Recalls Unify Assura ICDs for Security Firmware Update
St Jude Medical is recalling Unify Assura implantable cardiac devices to release new firmware that strengthens security against unauthorized access.
Product
Unify Assura, Sterile EO, Model #/ Part #: CD3257-40/100042333, 100059944; CD3257-40Q/100042334, 100059936; CD3261-40/100048460, 100048546, 100059897, 100059954, 100059996, 100078828; CD3261-40Q/100048568, 100048581, 100059898, 100059955, 100059997, 100078853…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2289-2018·2018-07-04
Zimmer Biomet Recalls Vanguard Knee Bearings Due to Packaging Mix-up
Zimmer Biomet is recalling 48 Vanguard Complete Knee System tibial bearings because two lots were commingled, creating a risk that 14mm bearings are packaged in 12mm boxes or vice versa.
Product
Vanguard Complete Knee System; E1 Vanguard PS Tibial Bearing; Model Numbers EP-183664, EP-183642 Product Usage: The product is intended for use in knee joint replacement arthroplasties.
Category
Medical Device
Distribution
18 states
HighFDA (Devices)·Z-2325-2018·2018-07-04
St Jude Medical Recalls Quadra Assura MP Implantable Cardiac Devices for Security Update
St Jude Medical is recalling 68,117 Quadra Assura MP implantable cardiac devices to release new firmware that strengthens security against unauthorized access.
Product
Quadra Assura MP, Sterile EO, Model #/ Part #: CD3269-40/100043177; CD3269-40Q/100043178; CD3271-40/100043130; CD3271-40Q/100043191; CD3369-40C/100080339, 100080478; CD3369-40Q/100080439, 100080476, 100105528; CD3371-40/100078814, 100079232, 100079513…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2324-2018·2018-07-04
St Jude Medical Recalls Quadra Assura ICDs for Security Firmware Update
St Jude Medical is recalling 72,673 Quadra Assura implantable cardiac devices to release new firmware that strengthens security against unauthorized access.
Product
Quadra Assura, Sterile EO, Model #/ Part #: CD3265-40/100042335, 100059846; CD3265-40Q/100042336, 100059847; CD3267-40/100042956, 100043569, 100059961, 100078810; CD3267-40Q/100043132, 100043539, 100059917, 100059956, 100078904; CD3365-40C/100080435, 100080436…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2328-2018·2018-07-04
St Jude Medical Recalls Unify Quadra ICDs for Security Firmware Update
St Jude Medical is recalling Unify Quadra implantable cardiac devices to release new firmware that strengthens security against unauthorized access.
Product
Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2312-2018·2018-07-04
Siemens Artis zee floor MN recalled for display failure
Siemens is recalling Artis zee floor MN systems because the display may fail to show images after power save mode, potentially requiring procedure cancellation.
Product
Artis zee floor MN, Material no. 10094142, for angiography and whole body radiographic/fluoroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2290-2018·2018-07-04
RayStation Radiation Therapy Software Recalled for Dose Calculation Accuracy Issues
RaySearch Laboratories is recalling RayStation Radiation Therapy Treatment Planning System software versions 6.0 through 7.0 because dose calculation accuracy may be less than expected in some situations.
Product
RayStation Radiation Therapy Treatment Planning System; 6.0, 6.1, 6.2, 7.0 Product Usage: Usage: RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans provide treatment unit set-up parameters and estimates of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2318-2018·2018-07-04
St Jude Medical Recalls Implantable Cardiac Devices for Security Firmware Update
St Jude Medical is recalling implantable cardiac devices to release new firmware that strengthens security against unauthorized access.
Product
Current, Sterile EO, Model #/ Part #: 1207-30/50020236-001, 60010739-207, 60010739-407; 1207-36/50020237-001, 60010742-207, 60010742-307, 60010742-407, 60010742-707; 2207-30/ 50020238-001, 60010738-207; 2207-36/ 50020239-001, 60010741-207, 60010741-307, 60010741-407…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2311-2018·2018-07-04
Siemens Artis zee floor recall due to display failure
Siemens is recalling 14 Artis zee floor systems because the display may fail to show images after power save mode, potentially requiring treatment cancellation.
Product
Artis zee floor, Material no. 10094135, for angiography and whole body radiographic/fluoroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide