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. 2,518 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,518 in last 12 months

Showing 2496124980 of 51,202 recalls

Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Airway Mobilescope MAF-TM Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-1T60 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchofiberscope BF-P60 Recalled by Olympus Corporation of the Americas Due...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-3C40 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-MP160F Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-P180 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Ultrasonic Bronchoscope BF-UC180F Recalled by Olympus Corporation of the...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-MP60 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-1T180 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchofiberscope BF-40 Recalled by Olympus Corporation of the Americas Due...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-1T40 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovidescope BF-1T240 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-P160 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-3C160 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugAugust 8, 2018· Hetero Labs Limited Unit V

Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2018· Akorn, Inc.

Recalled Item: Azelastine HCl Ophthalmic Solution 0.05% Recalled by Akorn, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications:out-of-specification (OOS)...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugAugust 8, 2018· Hetero Labs Limited Unit V

Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2018· Hetero Labs Limited Unit V

Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2018· Hetero Labs Limited Unit V

Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 8, 2018· Philips North America LLC

Recalled Item: Philips HeartStart Infant/Child SMART Pads Cartridge Recalled by Philips...

The Issue: The recall is being initiated due to incorrect age range labeling (8+ yrs)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing