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 27721–27740 of 51,202 recalls
Recalled Item: ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G....
The Issue: Package integrity failure observed during routine shift package integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImmunoCAP Allergen c6 Recalled by Phadia US Inc Due to The stability...
The Issue: The stability specifications of ImmunoCAP Allergen c6, Amoxicilloyl were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImmunoCAP Allergen c5 Recalled by Phadia US Inc Due to The stability...
The Issue: The stability specifications of ImmunoCAP Allergen c5, Ampicilloyl were not met.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular E 170 Analyzer: Immunoassay Chemistry Analyzer Recalled by Roche...
The Issue: Complaints have been received concerning questionable results on analyzers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas e 411 Immunoassay Analyzer (Discrete Photometric Analyzer for Clinical...
The Issue: Complaints have been received concerning questionable results on analyzers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: c6000 Recalled by Roche Diagnostics Corporation Due to Complaints have been...
The Issue: Complaints have been received concerning questionable results on analyzers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precedence 6 Model # 882351 Product Usage: Precedence (cleared as Recalled...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView Model 882480 Product Usage: BrightView and BrightView X are...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Model 882482 Product Usage: BrightView XCT is a Recalled by...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uterine Electromyographic Monitor - Monica Novii Wireless Patch System...
The Issue: if the cables of the Monica Novii System are removed by a user, and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uterine Electromyographic Monitor -Monica IF24 Interface System Product...
The Issue: if the cables of the Monica IF24 System are removed by a user, and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precedence 16 Model # 882350 Product Usage: Precedence (cleared as Recalled...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fosphenytoin Sodium Injection Recalled by Amneal Pharmaceuticals Due to...
The Issue: Presence of particulate matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.25% Acetic Acid Irrigation USP Recalled by B. Braun Medical Inc Due to...
The Issue: Presence of Particulate Matter: identified as polyethylene, which is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Oral Solution Recalled by Akorn Inc Due to CGMP Deviations:...
The Issue: CGMP Deviations: Inadvertent release of a drug product with unapproved...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shiseido Future Solutions LX Triple Points Bonus contains SPF 50+ Recalled...
The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shiseido Future Solution LX Luxurious Eye & Lip Collection contains Recalled...
The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shiseido Future Solution LX Discovery Set contains SPF 50+ (octinoxate 4.9%...
The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SPIRIVA HandiHaler (tiotropium bromide inhalation powder) 18 mcg/capsule (90...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.