State

Indiana product recalls

73,388 recalls have nationwide distribution and so reach Indiana. 9,587 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total: 9,587
Critical: 1,913
Severe: 2,528
Most recent: 2026-09-30

Of the 9,587 recalls naming Indiana we have scored against our rubric, 1,913 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,528 (26%) are Severe.

Which agencies issued them

These figures cover only the 9,587 recalls whose distribution notice names Indiana specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22476–22500 of 82975

HighFDA (Devices)·Z-1206-2022·2022-06-08
Medtronic cardiac catheter system recalled due to sterility barrier defect
Medtronic recalls its C304-HIS cardiac catheter device due to potential sterility barrier defects in certain manufacturing lots. Approximately 1,385 devices distributed worldwide were affected.
Product
The C304-HIS device features a guide wire to access the vein, a valve to reduce blood loss during the implant procedure, a deflectable catheter to introduce a transvenous device, a catheter dilator to facilitate deflectable catheter passage, and a guide catheter slitter to…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V404000·2022-06-08
2020-2022 Porsche Taycan center screen display malfunction increases crash risk
Porsche is recalling 2020-2022 Taycan vehicles for a software error causing the center screen and touch panel to go black or flicker. This blocks the driver's view of rear-view camera functions, increasing crash risk.
Product
PORSCHE — PORSCHE TAYCAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0956-2022·2022-06-08
Glycopyrrolate Injection Recalled Due to Lack of Sterility Assurance
Nephron is recalling 6,150 units of Glycopyrrolate Injection due to lack of sterility assurance. Healthcare providers should stop using affected lots and contact their supplier for return instructions.
Product
Glycopyrrolate Injection, USP, 0.6 mg/3 mL (0.2 mg/mL), Preservative Free, 3 mL Pre-Filled Syringe, 5 x 3 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-903-03
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1176-2022·2022-06-08
Core Biopsy Tray Recall Due to Manufacturing Validation Uncertainty
Busse Hospital Disposables is recalling Core Biopsy Trays (Catalog 8673R4) distributed nationwide because the test methods used to validate manufacturing processes may not have been adequately validated. The affected 285 units may lack proper quality verification.
Product
Core Biopsy Tray Catalog Number: 8673R4
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1157-2022·2022-06-08
I.V. Start Kit Recall Due to Uncertain Manufacturing Process Validation
Busse Hospital Disposables is recalling I.V. Start Kit (Catalog 8172) due to inadequate validation of manufacturing processes for the included swab drug products. The recall affects 4,218 units distributed nationwide.
Product
I.V. Start Kit Catalog 8172
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1152-2022·2022-06-08
Busse Single Shot Epidural Tray recalled for test method validation uncertainty
Busse Hospital Disposables is recalling Single Shot Epidural Trays nationwide due to uncertainty about the adequacy of test method validation used to manufacture swab components. The FDA classified this as a Class II recall.
Product
Single Shot Epidural Tray Catalog 1292
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1203-2022·2022-06-08
FDA Recalls Pellet Insertion Trays Due to Validation Method Uncertainty
Busse Hospital Disposables is recalling 3.2MM Pellet Insertion Trays due to inadequate validation of manufacturing test methods. The recall affects 150 units distributed nationwide.
Product
3.2MM Pellet Insertion Tray Catalog Number: B9743
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1174-2022·2022-06-08
Single Shot Epidural Tray Kits Recalled Due to Manufacturing Validation Uncertainty
Busse Hospital Disposables recalls Single Shot Epidural Tray kits due to uncertainty about the adequacy of test method validation in manufacturing. No illnesses reported.
Product
Single Shot Epidural Tray - 18G Catalog Number: 8139R2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0974-2022·2022-06-08
Losartan Potassium Tablets Recalled for CGMP Deviations and Elevated Impurity
Strides Pharma Inc. is recalling Losartan Potassium 100 mg tablets nationwide due to CGMP deviations with AZIDO impurity levels above acceptable limits. Patients should contact their healthcare provider to verify if they are affected.
Product
LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1143-2022·2022-06-08
Baxter Peritoneal Dialysis Manifold Sets Recalled for Lack of FDA Clearance
Baxter Healthcare Corporation is recalling 180 units of 5 Prong Manifold Sets used in peritoneal dialysis. These products were distributed without FDA regulatory clearance to facilities across nine US states.
Product
5 Prong Manifold Set (with Luer Connectors)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0957-2022·2022-06-08
Hydromorphone Injection Recalled Due to Lack of Sterility Assurance
Nephron Sterile Compounding Center is recalling Hydromorphone HCl Injection 50 mg/50 mL pre-filled syringes due to lack of sterility assurance. The recalled product was distributed nationwide.
Product
Hydromorphone HCl Injection, USP, 50 mg/50 mL (1 mg/mL), 50 mL Pre-Filled Syringe, 5 x 50 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-559-50
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0959-2022·2022-06-08
Ketamine Hydrochloride Injectable Recalled Due to Sterility Assurance Issues
Nephron Sterile Compounding Center LLC is recalling 30,290 syringes of Ketamine Hydrochloride Injection due to lack of assurance of sterility. The injectable drug was distributed nationwide.
Product
Ketamine Hydrochloride Injection, USP, 30 mg/3 mL (10 mg/mL), 3 mL Pre-Filled Syringe, 5 x 3 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-982-33
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1225-2022·2022-06-08
Hip Stem Prosthetic Missing Plasma Coating in Manufacturing Lot
MicroPort Orthopedics is recalling one manufacturing lot of PROFEMUR PLASMA Z CLASSIC hip stem prosthetics due to missing plasma-spray coating in the proximal region of the implant stem.
Product
PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0964-2022·2022-06-08
Oxytocin Injectable Drug Recalled for Lack of Sterility
Nephron Sterile Compounding Center has recalled 3,587 bags of Oxytocin injectable nationwide due to lack of assurance of sterility.
Product
Oxytocin 30 Units/500 mL (0.06 Units/mL) in 0.9% Sodium Chloride Injection, USP, 500 mL Single-Dose Container Bag, 10 x 1 IV Bag, Rx Only Nephron 503B outsourcing facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-543-50
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0958-2022·2022-06-08
Injectable Hydromorphone Recalled for Lack of Sterility Assurance
Nephron Sterile Compounding Center is recalling Hydromorphone HCl Injection due to lack of assurance of sterility. The recall affects 6,210 pre-filled syringes distributed nationwide.
Product
Hydromorphone HCl Injection, USP, 6 mg/30 mL (0.2 mg/mL), 30 mL Pre-Filled Syringe, 5 x 30 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-529-30
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0963-2022·2022-06-08
Neostigmine Methylsulfate Injection Recalled Due to Sterility Assurance Failure
Nephron Sterile Compounding Center is recalling Neostigmine Methylsulfate Injection due to lack of assurance of sterility. The compounded injectable drug may not meet sterile product standards.
Product
Neostigmine Methylsulfate Injection, USP, 5 mg/5 mL (1 mg/mL), Preservative Free, 5 mL Pre-Filled Syringe, 5 x 5 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only Nephron 503B outsourcing facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-902-05
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0976-2022·2022-06-08
AMBI Skincare Fade Cream Recalled for Temperature Storage Deviations
AMBI Skincare Fade Cream is being recalled nationwide due to cGMP violations. The product was stored outside its labeled temperature requirements during manufacturing.
Product
AMBI Skincare Fade Cream Normal Skin, Net Wt. 2 OZ. (56g)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1147-2022·2022-06-08
I.V. Start Kit with Swab Products Recalled for Manufacturing Validation Issues
Busse Hospital Disposables is recalling I.V. Start Kits containing swab products due to inadequate validation of manufacturing test methods. Approximately 2,475 units nationwide may be affected.
Product
I.V. Start Kit - Tegaderm Dressing - Catheter Securement - Prevantics Catalog Number: 822
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1213-2022·2022-06-08
Abbott FIRMap Catheter Recalled for Incorrect Product Labeling
Abbott is recalling 40 units of FIRMap® Catheter, 60mm Basket due to incorrect product labeling. The recall affects devices distributed in Missouri, California, Ohio, Washington and internationally in Italy and Netherlands.
Product
FIRMap" Catheter, 60mm Basket
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1180-2022·2022-06-08
Swab and Swabstick Drug Products Recalled Due to Validation Uncertainty
Busse Convenience kits with swab and swabstick drug products are being recalled because the validation of the test methods used during manufacturing is uncertain.
Product
"3.2MM Pellet Insertion Tray with Medium Gloves" Catalog Number: B1351
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1142-2022·2022-06-08
Locking Cap for PD Catheter Adapter Distributed Without FDA Clearance
Baxter Healthcare is recalling locking caps for peritoneal dialysis catheters that were distributed without FDA regulatory clearance. These devices were released into the U.S. market in error.
Product
Locking Cap for PD Catheter Adapter
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1193-2022·2022-06-08
Busse Convenience Kit Swab Products Recalled for Test Method Validation Issues
Busse Convenience kits containing swab and swabstick drug products manufactured by Professional Disposables International are being recalled due to uncertainty about test method validation during manufacturing.
Product
SS 4.5MM DIAMOND TIP TROCAR WITH MEDIUM GLOVES Catalog Number: B1560
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1195-2022·2022-06-08
Convenience Kits with Drug Swab Products Recalled for Validation Uncertainty
Busse Convenience kits containing swab/swabstick drug products are being recalled nationwide due to uncertainty about the adequacy of the validation of manufacturing test methods.
Product
Male SS 4.5MM Pellet Insertion Tray Catalog Number: B1570
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1184-2022·2022-06-08
Pellet Insertion Tray Recall for Uncertain Manufacturing Test Validation
Busse Hospital Disposables is recalling SS 3.5MM Pellet Insertion Tray kits nationwide. The kits contain swab products with uncertain manufacturing test method validation.
Product
SS 3.5MM Pellet Insertion Tray with Medium Gloves Catalog Number: B1354R1
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1144-2022·2022-06-08
Baxter Effluent Sample Bags Recalled for Lack of FDA Clearance
Baxter Healthcare recalled 78 Effluent Sample Bags that were distributed without FDA regulatory clearance. The product was distributed in error across eight states.
Product
Effluent Sample Bag
Category
Medical Device
Distribution
Distributed nationwide