Recalls affecting Indiana
Notices that name Indiana in their distribution area, plus every nationwide recall — nationwide recalls reach Indiana too.
-
Highest risk · 7 months ago
Good Brain Tonic 16 oz & 32 oz recall: Potential Foodborne Illness -Botulism
Potential Foodborne Illness -Botulism
-
NHTSA safety recall · 7 months ago
Hyundai recall: The driver and passenger seat belt anchors may detach
The driver and passenger seat belt anchors may detach.
-
Public Health Alert · 7 months ago
Dorada Foods FSIS Retracts Public Health Alert for Frozen recall: Product Contamination
Product Contamination
-
Class I · 7 months ago
Raw milk cheddar cheese, shredded and block recall: Potential Foodborne Illness – E. coli
Potential Foodborne Illness – E. coli
-
NHTSA safety recall · 7 months ago
General Chevrolet Malibu recall: The rearview camera screen may display a distorted or blank image
The rearview camera screen may display a distorted or blank image.
-
NHTSA safety recall · 7 months ago
BMW recall: The seal for the reverse gear control unit may deteriorate and allow moisture
The seal for the reverse gear control unit may deteriorate and allow moisture inside the control unit, which can result in the unit overheating.
-
NHTSA safety recall · 7 months ago
Volvo Trucks VNL and VNR recall: The vehicle turn signals may not function properly
The vehicle turn signals may not function properly. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety…
-
Class I · 7 months ago
Philips Respironics Trilogy Evo, Software Version 1.05.15.00 recall: Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators
Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume…
-
Class II · 7 months ago
Medline Industries, LP Puracol and Puracol Plus Collagen Wound Dressings: MSC8522 recall: Elevated endotoxin levels identified in affected lots. Issue may elicit
Elevated endotoxin levels identified in affected lots. Issue may elicit strong inflammatory response if used, including local tissue irritation…
-
Class II · 7 months ago
I.T.S. GmbH Pelvic Reconstruction System with the below descriptions recall: Updated MRI safety testing demonstrates higher RF-induced temperature
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the…
-
Class III · 7 months ago
Philips L12-5 Ultrasound Transducer recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
-
Class II · 7 months ago
Brand Name: Olympus Halo PKS Cutting Forceps recall: Olympus identified that the Cutting Forceps contain components
Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective…
-
Class II · 7 months ago
Beckman Coulter, Inc. MicroScan Neg MIC 56 REF C42464 UDI-DI code: 15099590731212 recall: Due to the likely presence of contamination in well(s)
Due to the likely presence of contamination in well(s).
-
Class II · 7 months ago
I.T.S. GmbH Volar Radius Plate with Angular Stability with the following recall: Updated MRI safety testing demonstrates higher RF-induced temperature
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the…
-
Class I · 7 months ago
Erbe USA Inc Flexible Cryoprobe REF: 20402-410. For surgical use recall: Probes may rupture/burst during activation
Probes may rupture/burst during activation
-
Class III · 7 months ago
Philips C9-4 Ultrasound Transducer recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
-
Class II · 7 months ago
Koven Technology, Inc. Brand Name: BiDop 3 Product Name: BiDop 3 Pocket Doppler recall: Product labeling includes a fetal indication for use that is not cleared
Product labeling includes a fetal indication for use that is not cleared under its 510(k).
-
Class II · 7 months ago
Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS recall: Olympus identified that the Cutting Forceps contain components
Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective…
-
Class II · 7 months ago
Brand Name: Olympus Everest Bipolar Cutting Forceps w/Cord recall: Olympus identified that the Cutting Forceps contain components
Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective…
-
Class II · 7 months ago
I.T.S. GmbH Pilonplate with Angular Stability, with the below descriptions recall: Updated MRI safety testing demonstrates higher RF-induced temperature
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the…
-
Class III · 7 months ago
Philips X7-2 Ultrasound Transducer recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
-
Class III · 7 months ago
Philips 3D6-2 Ultrasound Transducer recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
-
Class II · 7 months ago
I.T.S. GmbH FR.O.H. Calcaneus Repair System with the following description recall: Updated MRI safety testing demonstrates higher RF-induced temperature
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the…
-
Class II · 7 months ago
Custom Abutment AS Ti, for Straumann RC, incl. TAN screw recall: A material mix-up had occurred during the manufacturing of Straumann¿ Custom
A material mix-up had occurred during the manufacturing of Straumann¿ Custom Abutments. More specifically, a raw material bar of TAN-material (SAP…