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.

51,202 total recalls
2,506 in last 12 months

Showing 2818128200 of 51,202 recalls

DrugOctober 19, 2017· Allergan Sales, LLC

Recalled Item: Combigan (brimonidine tartrate/timolol maleate ophthalmic solution)...

The Issue: Failed Impurities/Degradation Specifications.

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 24202 ADULT ECC Recalled by Datascope Corporation Due to The Better...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 27610 ECC PACK 3/8 Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 22300 Recalled by Datascope Corporation Due to The Better Bladder...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 22702 ECC W/HMOD 30000 Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Cook Inc.

Recalled Item: Mallinckrodt Institute Percutaneous Gastrostomy Set Product Usage: Intended...

The Issue: Cook has identified that the affected lots may contain wire guides that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-T 25502 1/4 Better Bladder Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 49101 Childrens Large ECC Pack Recalled by Datascope Corporation Due...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 50900 Custom ECC Pack-Neonatal 1/4 Recalled by Datascope Corporation...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: NICU ECC Pack BEQ-TOP 39202 Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 50903 Custom ECC Pack-Pedriatric Recalled by Datascope Corporation...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 33500 3/8" ECC PACK Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Cook Inc.

Recalled Item: Percutaneous Gastrojejunostomy Set Product Usage: Intended for the...

The Issue: Cook has identified that the affected lots may contain wire guides that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-T 25501 3/8" Better Bladder Pack Recalled by Datascope Corporation Due...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Cook Inc.

Recalled Item: Wills-Oglesby Percutaneous Gastrostomy Set Product Usage: Intended for the...

The Issue: Cook has identified that the affected lots may contain wire guides that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 22701 Recalled by Datascope Corporation Due to The Better Bladder...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR Recalled by Johnson &...

The Issue: Some contact lenses were associated with complaints of a foreign matter...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 38900 ECC PACK Recalled by Datascope Corporation Due to The Better...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS Recalled by Johnson &...

The Issue: Some contact lenses were associated with complaints of a foreign matter...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: 1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses Recalled by Johnson...

The Issue: Some contact lenses were associated with complaints of a foreign matter...

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

Class II — Potential Health HazardOngoing