State

Indiana product recalls

72,940 recalls have nationwide distribution and so reach Indiana. 9,555 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total: 9,555
Critical: 1,903
Severe: 2,136
Most recent: 2026-09-09

Of the 9,555 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 9,555 recalls whose distribution notice names Indiana specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3776–3800 of 82495

ModerateFDA (Devices)·Z-1050-2026·2026-01-21
Open heart kits recalled because they contain recalled B. Braun administration sets
Medline is recalling 633 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) OPEN HEART ACCESSORY CDSKit SKU CDS984289O; 2) OPEN HEART CDSKit SKU CDS984355K; 3) BAG A OPEN HEART KITKit SKU DYKM1025D; 4) RR-CABG SUPPLEMENTAL PACKKit SKU DYNJ0394752
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1051-2026·2026-01-21
Pre-op kits recalled because they contain recalled B. Braun administration sets
Medline is recalling 32 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) DELUXE PRE OP KIT, Medline SKU DYKS2034A; 2) DELUXE PRE OP KIT, Medline SKU DYKS2006B.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1065-2026·2026-01-21
Allura Xper FD10/10, model 722005, recalled over a missing drip tray
Philips Medical Systems Nederland is recalling 14 units of the Allura Xper FD10/10, model 722005, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD10/10; Model Number: 722005;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1088-2026·2026-01-21
Robotic and gynaecology kits recalled over leaking suction irrigators inside
Medline is recalling 12,584 procedure convenience kits containing Stryker Strykeflow 2 Suction Irrigators, which can leak or emit vaporized saline during use.
Product
Medline medical procedure convenience kits labeled as: 1) ROBOTIC, REF CDS980523M; 2) ROBOTIC GYN, REF CDS980647K; 3) DAVINCI PROCEDURE, REF CDS980864Q; 4) GYN-URO LAPSCP CDS-LF, REF CDS981583U; 5) GYN-URO LAPSCP CDS-LF, REF CDS981583V; 6) GYN ROBOTIC, REF CDS981826K
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1075-2026·2026-01-21
Allura Xper FD20, model 722028, recalled over a missing drip tray
Philips Medical Systems Nederland is recalling 2 Allura Xper FD20 systems because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD20; Model Number: 722028;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1056-2026·2026-01-21
IV start kits recalled over recalled B. Braun administration sets inside
Medline is recalling 5314 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) IV START KIT NS, Medline kit SKU DYKM1980C; 2) (134) L&D IV-START SET, Medline kit SKU DYKM2137B; 3) IV START KIT, Medline kit SKU DYKS1372C; 4) IV START KIT, Medline kit
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1077-2026·2026-01-21
Allura Xper FD20/20 systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 8 units of the Allura Xper FD20/20, model 722038, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD20/20; Model Number: 722038;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0257-2026·2026-01-21
Clindamycin topical solution recalled after failing impurity and assay specifications
Sun Pharmaceutical Industries is recalling Clindamycin Phosphate Topical Solution 1% after out of specification results for total impurities and for assay.
Product
CLINDAMYCIN PHOSPHATE — CLINDAMYCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1043-2026·2026-01-21
Neurostimulator clinician programmer app recalled over faults during device use
Medtronic is recalling 7,123 units of the Vanta Clinician Programmer Application after complaints that it does not function as intended during use.
Product
A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software is deployed and operated on Samsung tablets (CFN CT900).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1053-2026·2026-01-21
Donor nephrectomy accessory kits recalled over recalled B. Braun sets
Medline is recalling 33 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: RR-LAP DONOR NEP ACCESSORY, Medline kit SKU DYNJ63395B
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1063-2026·2026-01-21
Allura Xper FD10F systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 12 units of the Allura Xper FD10F, model 722002, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD10F; Model Number: 722002;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0274-2026·2026-01-21
Admission and admin kits recalled over recalled B. Braun administration sets
Medline is recalling 1725 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
CHILDREN NYQUIL, COLD&FLU, BERRY, 8oz, 12ct
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0280-2026·2026-01-21
PALACOS MV plus G bone cement recalled because ampoules may not break
Heraeus Medical is recalling PALACOS MV+G pro 40 and PALACOS MV+G pro 80 bone cement because an unfortunate combination of factors can leave ampoules unbroken, so no appropriate cement dough is formed.
Product
Swan, White Clear Alcohol, 50%, 16oz, 12 count
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0259-2026·2026-01-21
Carotid anesthesia kits recalled over recalled B. Braun administration sets inside
Medline is recalling 10 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1091-2026·2026-01-21
Azurion systems recalled over six identified software issues
Philips Medical Systems Nederland is recalling 10,466 Azurion systems on software versions R2.1.10 and R2.2.10 over six identified software issues including continuous restart.
Product
Philips Azurion Systems with software versions R2.1.10 and R2.2.10. Includes the following label descriptions and corresponding models: 1. Azurion 3 M12. Model Numbers: 722063, 722221. 2. Azurion 3 M15. Model Numbers: 722064, 722222, 722280. 3. Azurion 5 M12. Model Num
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1059-2026·2026-01-21
Neuro angio packs recalled over recalled B. Braun administration sets inside
Medline is recalling 12 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: NEURO ANGIO PACK, Medline kit SKU DYNJ38935
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1060-2026·2026-01-21
Allura Xper FD10 systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 56 units of the Allura Xper FD10, model 722010, because the drip tray beneath the cooling unit may not have been installed.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) RR-PLASTIC CRANIOFACIAL PK-LF, Medline kit SKU DYNJ0395085V; 2) NH PERI DISC PACK, Medline kit SKU DYNJ66311C; 3) DISCECTOMY PACK, Medline kit SKU DYNJ86770; 4) TOTAL KNEE
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1073-2026·2026-01-21
Allura Xper FD20 Biplane, model 722013, recalled over a missing drip tray
Philips Medical Systems Nederland is recalling 23 units of the Allura Xper FD20 Biplane, model 722013, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD10; Model Number: 722026;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1064-2026·2026-01-21
Allura Xper FD10, model 722003, recalled over a missing drip tray
Philips Medical Systems Nederland is recalling 93 units of the Allura Xper FD10, model 722003, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD10; Model Number: 722003;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1076-2026·2026-01-21
Preoperative kits recalled over recalled B. Braun administration sets inside
Medline is recalling 11173 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
Allura Xper FD20/10; Model Number: 722029;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1072-2026·2026-01-21
Allura Xper FD20 OR Table recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 4 units of the Allura Xper FD20 OR Table, model 722023, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD20 OR Table; Model Number: 722023;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1017-2026·2026-01-21
Allura Xper FD20 systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 79 units of the Allura Xper FD20, model 722012, because the drip tray beneath the cooling unit may not have been installed.
Product
VANTAGE GALAN 3T Model MRT-3020/MEXL-3020
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1068-2026·2026-01-21
Allura Xper FD10, model 722026, recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 95 units of the Allura Xper FD10, model 722026, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD10; Model Number: 722010;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1049-2026·2026-01-21
Allura Xper FD20/10 systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 4 units of the Allura Xper FD20/10, model 722029, because the drip tray beneath the cooling unit may not have been installed.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: AN01 CAROTID ANESTH KIT-LF, Medline Kit SKU PHS972096014B
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0256-2026·2026-01-21
Fluocinolone topical solution recalled after failing an impurity specification
Sun Pharmaceutical Industries is recalling 24,624 bottles of Fluocinolone Acetonide Topical Solution 0.01% after an out of specification result for a known impurity.
Product
FLUOCINOLONE ACETONIDE — FLUOCINOLONE ACETONIDE (FLUOCINOLONE ACETONIDE)
Category
Drug
Distribution
Distributed nationwide