State

Indiana product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49301–49325 of 83422

ModerateFDA (Devices)·Z-1715-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi EndoWrist Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpreted instructions may cause tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Danish SRK. General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1721-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi EndoWrist Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi German SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0632-2017·2017-04-12
Alvogen Recalls Adalat CC Tablets Due to Sorafenib Cross-Contamination
Alvogen, Inc. is recalling specific lots of Adalat CC (nifedipine) Extended-Release Tablets due to cross-contamination with sorafenib powder.
Product
Adalat CC (nifedipine) Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Manufactured for Almatica Pharma Inc. Pine Brook, NJ 07058 USA, NDC 50419-70305
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1728-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Spanish SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci¿…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1708-2017·2017-04-12
Philips eCare Coordinator Software Recalled for Data Integrity Defects
Philips Visicu is recalling eCare Coordinator software due to a defect that may cause missing or redundant data to be saved without user notification.
Product
eCare Coordinator Product Usage: is software intended for use in data aggregation, patient interaction facilitation, storage and clinical information management with independent physiological devices and ancillary systems that are connected either directly or through…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0631-2017·2017-04-12
Alvogen Recalls Nifedipine Tablets Due to Sorafenib Cross-Contamination
Alvogen Inc. is recalling Nifedipine Extended-Release Tablets, 90 mg, due to cross-contamination with sorafenib powder found in the inlet air duct.
Product
Nifedipine Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-370-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1706-2017·2017-04-12
Philips Recalls Mobile Diagnostic X-Ray Systems Due to Marker Placement Error
Philips Healthcare Inc. is recalling 220 Mobile Diagnostic X-Ray Systems because electronic markers may be placed at the wrong anatomical position when images are moved between views.
Product
Mobile Diagnostic X-Ray System with Digital Panel
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1719-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits Due to Instruction Errors
Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi French SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1723-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits Due to Instruction Issues
Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpreted instructions may cause tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Japanese SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1717-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Dutch SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci¿…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1716-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi EndoWrist Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Czech SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci¿…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1714-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi English SRK.. General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1726-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpreted instructions may cause tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Portuguese SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0629-2017·2017-04-12
Adalat CC Tablets Recalled for Sorafenib Cross-Contamination
Alvogen, Inc. is recalling Adalat CC (nifedipine) Extended Release Tablets due to cross-contamination with sorafenib powder found in the manufacturing facility.
Product
Adalat CC (nifedipine) Extended Release Tablets, 60 mg, 100- count bottles, Rx only Manufactured for Almatica, Almatica Pharma Inc. Pinebrook, NJ 07058 USA, NDC 50419-702-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0628-2017·2017-04-12
Adalat CC Tablets Recalled for Sorafenib Cross-Contamination
Alvogen, Inc. is recalling Adalat CC (nifedipine) Extended Release Tablets 30 mg due to cross-contamination with sorafenib powder.
Product
Adalat CC (nifedipine) Extended Release Tablets 30 mg, 100-count bottles, Rx only, Manufactured for Bayer Healthcare Bayer Healthcare Pharmaceuticals Inc. Whippany, NJ 07901 Manufactured in Germany, NDC 50419-701-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1724-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Italian SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1722-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi EndoWrist Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Greek SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci¿…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0627-2017·2017-04-12
Alvogen Recalls Nifedipine Extended-Release Tablets Due to Sorafenib Cross-Contamination
Alvogen, Inc. is recalling Nifedipine Extended-Release Tablets, 30 mg, due to cross-contamination with sorafenib powder found in the manufacturing facility's inlet air duct.
Product
Nifedipine Extended-Release Tablets, 30 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-368-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1753-2017·2017-04-12
Philips BrightView X Gamma Camera Recall Due to Brake Hub Assembly Error
Philips Medical Systems is recalling 27 BrightView X gamma cameras because a brake hub assembly error can cause the detector to backdrive.
Product
BrightView X 3/8 model number 882478 BrightView and BrightView X are gamma cameras designed for single or dual detector nuclear imaging accommodating a broad range of Emission Computed Tomography (ECT) studies. The cameras can be used to perform planar static, dynamic, gated…
Category
Medical Device
Distribution
29 states
ModerateFDA (Drugs)·D-0647-2017·2017-04-12
Fresenius Kabi Recalls Subpotent Fluphenazine Decanoate Injection Vials
Fresenius Kabi USA is recalling 118,224 vials of Fluphenazine Decanoate Injection because the drug was found to be subpotent.
Product
Fluphenazine Decanoate Injection, USP; 25 mg/mL, 5mL vials, Rx only, APP Pharmaceuticals, LLC Schaumburg, IL 60173, NDC 63323-0272-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1729-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi EndoWrist Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Turkish SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci¿…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1718-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi EndoWrist Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Finnish SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1748-2017·2017-04-12
Siemens ADVIA Centaur BR Assay Recalled for Potential Interference
Siemens Healthcare Diagnostics is recalling ADVIA Centaur BR assays due to potential interference from the Syphilis assay on the same systems.
Product
Siemens ADVIA Centaur BR assay Cat No. 03896216, SMN 10334837 (5-pack/250 tests) BR Assay for CA 27.29 The ADVIA Centaur¿ BR assay is an in vitro diagnostic test for the quantitative serial determination of cancer antigen CA 27.29 in human serum using the ADVIA Centaur¿…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0650-2017·2017-04-12
Lupin Recalls Quinapril Tablets Due to Impurity A Specification Failure
Lupin Pharmaceuticals is recalling Quinapril 5 mg tablets because they failed impurity specifications. The recall covers 15,168 bottles distributed nationwide.
Product
QUINAPRIL — QUINAPRIL (QUINAPRIL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0634-2017·2017-04-12
Alvogen Recalls Adalat CC Tablets Due to Sorafenib Cross-Contamination
Alvogen, Inc. is recalling Adalat CC (nifedipine) 60 mg extended-release tablets because residual sorafenib powder was found in the manufacturing facility's inlet air duct.
Product
Adalat CC (nifedipine) Extended-Release Tablets, 60 mg, 100-count bottles, Rx Only, Manufactured for Almatica Pharma Inc. Pine Brook, NJ 07058 USA, NDC 5242749501
Category
Drug
Distribution
Distributed nationwide