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. 1,097 recalls have been distributed to Indiana in the last 12 months.
Showing 15581–15600 of 53,528 recalls
Recalled Item: BD Extension Set SMALLBORE Tubing SmartSite VALVE Recalled by CAREFUSION Due...
The Issue: Needle-free connector valves, either standalone or attached to extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES Recalled by...
The Issue: Needle-free connector valves, either standalone or attached to extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Pump Infusion Buerette Set Smallbore Tubing Smartsite Port...
The Issue: Needle-free connector valves, either standalone or attached to extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: uEXPLORER PET/CT System - Product Usage: intended to be operated Recalled by...
The Issue: The EXAM acquisition workflow could occasionally freeze after canceling the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Gravity Burette Set 60 DP 3 SmartSite VALVES BALL VALVE DRIP CHAMBER...
The Issue: Needle-free connector valves, either standalone or attached to extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD SmartSite Bag Access Device Recalled by CAREFUSION Due to Needle-free...
The Issue: Needle-free connector valves, either standalone or attached to extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOND Ready-To-Use Primary Antibody CDX2 (EP25) Recalled by Leica...
The Issue: Product may not perform as specified in IFU.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phantom Nail System Recalled by Paragon 28, Inc. Due to A thin wall...
The Issue: A thin wall condition between the inner cannulation and the flutes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T Evoluton- Magnetic Resonance Medical Electrical Systems...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S-Magnetic Resonance Medical Electrical Systems indicated...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia CX 3.0T-Magnetic Resonance Medical Electrical Systems indicated for...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition X-Magnetic Resonance Medical Electrical Systems indicated...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T-Magnetic Resonance Medical Electrical Systems indicated for use...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arjo Disposable Repositioning Sling Recalled by Getinge Dominican Republic...
The Issue: Sling loop straps on device pose a trip hazard.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Combipatch (estradiol/norethindrone acetate transdermal system) 0.05/0.14 mg...
The Issue: Failed Stability Specifications; out of specification for shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Combipatch (estradiol/norethindrone acetate transdermal system) 0.05/0.25 mg...
The Issue: Failed Stability Specifications; out of specification for shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FLUDARABINE PHOSPHATE FOR INJECTION Recalled by Custopharm, Inc. Due to Lack...
The Issue: Lack of Assurance of Sterility: the manufacturing firm had microbial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Octreotide Acetate Injection 1000 mcg/5mL Recalled by Teva Pharmaceuticals...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.