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. 1,074 recalls have been distributed to Louisiana in the last 12 months.
Showing 11241–11260 of 29,201 recalls
Recalled Item: Biomet ARTHROSIMPLICITY KIT EU Item Number: 24-4055 Recalled by Biomet, Inc....
The Issue: Product not properly being aligned with the adequate gamma sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) RingLoc Bi-Polar Hip System Acetabular Cup ArCom: Acetabular Bi-Polar...
The Issue: Zimmer Biomet is conducting a medical device recall for three lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CarePoint 60 mL Syringe Without Needle Recalled by Allison Medical, Inc. Due...
The Issue: Syringe without needle may have a green substance on the plunger. Substance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate with Taper...
The Issue: Product potentially being packaged without a taper adapter or baseplate. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Langston Dual Lumen Catheter. Recalled by Vascular Solutions, Inc. Due to...
The Issue: The inner lumen of the Langston catheter may separate from the hub during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BenchMark ULTRA Advanced Staining System (IVD)- Material Number: 05342716001...
The Issue: Potential for Fluid leaks within the instruments, creating an electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PermaFlo Flowable Composite 948 Shade: A2 - Product Usage: Recalled by...
The Issue: Due to a potential manufacturing issue (cross contamination), composite is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinning Spiros Recalled by ICU Medical, Inc. Due to Potential for spinning...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3mL Syringe w/Spinning Spiros Recalled by ICU Medical, Inc. Due to Potential...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AltiVate Reverse Small Socket Insert Recalled by Encore Medical, LP Due to...
The Issue: Product mislabeled. Use may result in a delay in surgery, stopping of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 31" (78 cm) Appx 3.4 ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinning Spiros Closed Male Luer Recalled by ICU Medical, Inc. Due to...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 3.2 ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 76 cm (30") Appx 3.3 ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Appx 1.7 ml Bag Spike w/Integrated Clave Recalled by ICU Medical, Inc. Due...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 IN (13 cm) Appx 1.5 ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 5.5 mL 20 Drop Admin Set w/Integrated Clave Drip Chamber...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spiros CLOSED MALE LUER w/RED CAP Recalled by ICU Medical, Inc. Due to...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 42 IN (107 cm) Appx 5.0 ml Recalled by ICU Medical, Inc. Due to Potential...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 26 IN(66 cm) APPX 3.4ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.