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. 2,506 recalls have been distributed to Louisiana in the last 12 months.
Showing 29181–29200 of 51,202 recalls
Recalled Item: AVID TruCustom GYN LAPAROSCOPY convenience kits Recalled by Avid Medical,...
The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVID TruCustom UPPER EXTREMITY convenience kits Recalled by Avid Medical,...
The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVID TruCustom DJ'S VASCULAR/NEURO TRAY convenience kits Recalled by Avid...
The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVID TruCustom LAMINECTOMY PACK convenience kits Recalled by Avid Medical,...
The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVID TruCustom ELECTRO PHYSIOLOGY PK convenience kits Recalled by Avid...
The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVID TruCustom PACEMAKER TRAY convenience kits Recalled by Avid Medical,...
The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVID TruCustom PV MINOR PACK convenience kits Recalled by Avid Medical, Inc....
The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InflammaDry(R) AN RPS DIAGNOSTIC SOLUTION Recalled by Quidel Corporation Due...
The Issue: In-house testing revealed the presence of plastic spurs at the tips of some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Pressure Disposable Pressure Display Sets Extends the pressure line...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Antegrade/Retrograde Adapter Method for perfusion of cardioplegia...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Cardioplegia Adapter with Pressure Port Provides access for a Recalled...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Pressure Monitoring Extension Line Adapters Extends the pressure line...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Extension Line Adapters 20 in length Used to extend Recalled by...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Potassium PHOSphate added to 0.9% Sodium Chloride 250 mL Bag Recalled by SCA...
The Issue: Lack of sterility assurance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate added to 250 mL 0.9% Sodium Chloride 15 Recalled by SCA...
The Issue: Lack of sterility assurance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate added to 250 mL 0.9% Sodium Chloride 15 Recalled by SCA...
The Issue: Lack of sterility assurance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate added to 250 mL 0.9% Sodium Chloride 10 Recalled by SCA...
The Issue: Lack of sterility assurance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spinal & Epidural Anesthesia Tray. Product Catalog Number: 555172. Local...
The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perifix Continuous Epidural Anesthesia Tray. Product Catalog Numbers: 332075...
The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perifix Epidural AnesthesiaTray. Product Catalog Numbers: 551879 Recalled by...
The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.