Product Recalls in Indiana
Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,729 recalls have been distributed to Indiana in the last 12 months.
Showing 8681–8700 of 29,228 recalls
Recalled Item: Comprehensive Shoulder System Primary Shoulder Stem Recalled by Biomet, Inc....
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition X (Product Number 781356) - HA FlexTrak II Recalled by...
The Issue: Magnetic materials were used for the wheels of trolley. Wheels with magnetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T (Product Number 781396) - HA FlexTrak II (Accessory Recalled by...
The Issue: Magnetic materials were used for the wheels of trolley. Wheels with magnetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition X (Product Number 781358) - HA FlexTrak II Recalled by...
The Issue: Magnetic materials were used for the wheels of trolley. Wheels with magnetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Luer Lok Access Device - intended as a sterile Recalled by...
The Issue: May shed contaminant particles into the urine specimen that may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXCERA SMILE -a Dental resins for the fabrication of artificial teeth...
The Issue: Manufactured in a non-FDA-registered manufacturing facility and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXCERA BASE -a Dental resins for the fabrication of artificial teeth...
The Issue: Manufactured in a non-FDA-registered manufacturing facility and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 12MM-intended as a Recalled...
The Issue: May have adhesive residue on the posterior surface of the femoral augment,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE REVISION DISTAL FEMORAL AUGMENT SZ 6 4MM- Intended as Recalled by...
The Issue: May have adhesive residue on the posterior surface of the femoral augment,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor Plus Analyzer - intended to provide rapid test Recalled by Becton...
The Issue: May have the potential to overheat and/or cause fire, the issue can occur...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Optima Coil System consists of an implantable embolization coil Recalled...
The Issue: Due to Label/Pouch mix-up. Pouches incorrectly labeled. Incorrect shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRA SURFIX ALPHA Screwdriver Torx 10 Recalled by Smith & Nephew, Inc....
The Issue: The affected screwdrivers are out of specification and may not mate with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eCareManager version 4.2.1 Recalled by Philips North America Llc Due to...
The Issue: eCareManager (eCM) Sentry Score software not approved for use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRYPTOCOCCAL ANTIGEN LATERAL FLOW ASSAY Recalled by Immuno-Mycologics, Inc...
The Issue: The firm found immunoassay products used to detect cryptococcal antigen in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation/RayPlan- designed for treatment planning and analysis of...
The Issue: If a new primary image set is selected while the cine loop is running, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE Micro-Kill Bleach Germicidal Bleach Wipes Recalled by MEDLINE...
The Issue: Micro-Kill Bleach Wipes contain out of specification (low) levels of Sodium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDPOR Titan OFW - MTB - Right - 1.0mm Recalled by Stryker Leibinger GmbH &...
The Issue: Inside the packaging of one reported item a non-conforming product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Spectrum IQ Infusion Pumps Recalled by Baxter Healthcare Corporation...
The Issue: There is the potential for reduced or non-delivery of medication, in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)...
The Issue: There is the potential for reduced or non-delivery of medication, in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchial Microbiology Brush Recalled by Hobbs Medical, Inc. Due to The...
The Issue: The labeling for the Microbiology Brush identifies the device as a Bronchial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.