Product Recalls in Louisiana
Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,678 recalls have been distributed to Louisiana in the last 12 months.
Showing 7241–7260 of 51,202 recalls
Recalled Item: Calibration Serum Level 3 CAL2351 Recalled by Randox Laboratories Ltd. Due...
The Issue: CK Total in Calibration Serum Level 3, CAL2351, is running with a positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (5.4 mm diameter) Model:...
The Issue: Instructions for Use-User Deviations related to the reprocessing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protege GPS Self-Expanding Peripheral Stent System Recalled by Medtronic...
The Issue: Seal defects could compromise the ability of the product packaging to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (10 mm diameter) Model:...
The Issue: Instructions for Use-User Deviations related to the reprocessing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard Dressing change kit Recalled by ROi CPS LLC Due to ROi CPS...
The Issue: ROi CPS manufactured and distributed medical convenience kits with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KeySplint Hard Clear - Indicated for the fabrication of orthodontic Recalled...
The Issue: Keyprint Keysplint Hard Clear 1 kg resin bottles were inadvertently packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirTouch F20 Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirTouch N20 Nasal Mask and User Guide Recalled by ResMed Ltd. Due to Masks...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFit F30 Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFit N10 Nasal Masks and User Guide Recalled by ResMed Ltd. Due to Masks...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFit F20 Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFit F30i Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFit N20 Nasal Mask and User Guide Recalled by ResMed Ltd. Due to Masks...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vigabatrin for Oral Solution Recalled by InvaGen Pharmaceuticals, Inc. Due...
The Issue: Defective Container: powder may leak out of the pouch
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Panorama 1.0T HFO Recalled by Philips North America Llc Due to Firm was...
The Issue: Firm was informed of an event in which the structural integrity of the MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AbsorbaTack Absorbable Fixation Device 30 Violet Absorbable Tacks 5 mm-...
The Issue: Packaging of the device may cause a low seal strength in the side seal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V. Mueller Universal Bandage Scissors Black Plastic Handles Heavy-Duty...
The Issue: Bandage Scissors handle cover component contains an incorrect color...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL...
The Issue: An incorrect stopper was used in nine lots of 10mL BD PosiFlush Normal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Valleylab FT10 Recalled by Covidien Due to Due to software issue,...
The Issue: Due to software issue, New systems may exhibit an error which may prohibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frozen Recalled by Raw Seafoods Inc. Due to Undeclared Sesame
The Issue: Contains undeclared sesame seeds and milk
Recommended Action: Do not consume. Return to store for a refund or discard.