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. 1,041 recalls have been distributed to Louisiana in the last 12 months.
Showing 16881–16900 of 51,202 recalls
Recalled Item: Cascade Abrazo aPTT Test Card - Product Usage: are to Recalled by Helena...
The Issue: Intermittent potential for shorter than expected clot times.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NA-201SX-4022-C ASPIRATION NEEDLE ViziShot 22G w/o stylet Recalled by Aomori...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX LOWER 23G 5MM Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 21G 4MM Recalled by Aomori Olympus Co., Ltd....
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEEDLEMASTER 4MMx 26G UPPER Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NA-411D-1521 ASPIRATION NEEDLE Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SD-210U-10 ELECTROSURGICAL SNARE Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX 25G 2.5MM Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KD-611L ELECTROSURGICAL KNIFE Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-202 GUIDE SHEATH KIT 2.0MM Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEEDLEMASTER 3MMx 23G LOWER Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SD-230U-20 ELECTROSURGICAL SNARE Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PR-V614M 2-LUMEN CANNULA Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B7-2LA BALLOON CATHETER 13MM DIA 3.2 Recalled by Aomori Olympus Co., Ltd....
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 23G 6MM Recalled by Aomori Olympus Co., Ltd....
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 25G 6MM Recalled by Aomori Olympus Co., Ltd....
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 21G 6MM Recalled by Aomori Olympus Co., Ltd....
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KD-620UR ELECTROSURGICAL SNARE Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX LOWER 25G 6MM Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX LOWER 23G 3MM Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.