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 28241–28260 of 51,202 recalls
Recalled Item: Triple Chocolate Mudslide Cookie Recalled by Midway Specialty Vehicles LLC...
The Issue: Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate Chip-N-Chunk Cookie Recalled by Midway Specialty Vehicles LLC Due...
The Issue: Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Red Velvet Cookie Recalled by Midway Specialty Vehicles LLC Due to...
The Issue: Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clofarabine injection Recalled by Sanofi-Aventis U.S. LLC Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Package Insert: authorized generic product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clolar (clofarabine) 20 mg/20 mL (1 mg/mL) Injection Recalled by Genzyme...
The Issue: Labeling: Incorrect or Missing Package Insert.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carestation 620 A1 Recalled by GE Medical Systems China Co., Ltd. Due to...
The Issue: Possible incomplete seal between the CO2 absorber and the breathing circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TunneLoc Tibial Fixation Device (Within an ACL Kit) Product Usage: Recalled...
The Issue: Gamma sterilization validation testing indicates the sterilization dose for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arkon Anesthesia Delivery System Recalled by Spacelabs Healthcare, Ltd. Due...
The Issue: Arkon Anesthesia Workstation, with software version 2.61, experienced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TunneLoc Tibial Fixation Device Product Usage: To provide fixation of...
The Issue: Gamma sterilization validation testing indicates the sterilization dose for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestation 620 A2 Recalled by GE Medical Systems China Co., Ltd. Due to...
The Issue: Possible incomplete seal between the CO2 absorber and the breathing circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Tapered SwissPlus & SwissPlus Implant Systems surgical kit...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental GemLock RHD2.5 Hex Driver. The label shows the Recalled by...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crimson Trace Corporation laser sights. The Finished Products are laser...
The Issue: A previously "in specification" Finished Product with a Model 25-0657 diode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STORZ High Flow Insufflation Tubing (with filter) Recalled by Karl Storz...
The Issue: The label outside the cardboard box is labeled correctly but the pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Legacy(TM) 3 Implant Recalled by Implant Direct Sybron...
The Issue: One reported complaint and discovered that the outer vial was out of round...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norepinephrine Bitartrate 8 mg added to 0.9% Sodium Chloride 250 mL in a bag...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem HCL 125 mg added to 0.9% Sodium Chloride 100 ml bag Recalled by...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Succinylcholine 200 mg/10 mL Syringe Recalled by Banner Pharmacy Services,...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.