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. 1,129 recalls have been distributed to Indiana in the last 12 months.
Showing 7381–7400 of 29,228 recalls
Recalled Item: Flow-c Anesthesia System (Product Code 6887700) Flow-e Anesthesia System...
The Issue: The power backup battery, under certain conditions, may exhibit reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R&D CBC-3D Hematology Control: (1) CBC-3D Normal Pack Hematology Control...
The Issue: For one lot of CBC-3D Hematology Control, the Normal Level may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis Angiographic Catheter Extensions. Used to transport fluid from the...
The Issue: There is a potential for separation at the male connector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests (600T)-...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests Japan...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HF Resection Electrodes Recalled by Olympus Corporation of the Americas Due...
The Issue: An incompatible HF cable may be packaged with the HF Resection Electrodes....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests OUS...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Action INDUSTRIES INC. Port a Cath Kit Recalled by Medical Action...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VADER Pedicle System Torque Wrench Recalled by Icotec Ag Due to During...
The Issue: During internal testing (at manufacturer site) of two torque wrench devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS Recalled...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total...
The Issue: Due to tears reported tears in the cannula due to wear and tear stress.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carefusion V. Mueller" HARDY-STYLE BAYONET BIPOLAR FORCEPS Recalled by...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carefusion V. Mueller CUSHING BAYONET BIPOLAR FORCEPS Recalled by Carefusion...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller TITANIUM BAYONET BIPOLAR FORCEPS Recalled by...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller TITANIUM BAYONET INSULATED IRRIGATING BIPOLAR FORCEPS...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller TITANIUM BAYONET BIPOLAR FORCEPS Recalled by...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carefusion V. Mueller Neuro/Spine JEWELERS BIPOLAR FORCEPS 0.4MM TIP...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carefusion V. Mueller CUSHING BIPOLAR FORCEPS 1.5MM TIP Recalled by...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carefusion V. Mueller ADSON BIPOLAR FORCEPS 1.0MM TIP OVERALL LENGTH...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.5MM TIP...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.