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. 2,646 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,646 in last 12 months

Showing 1328113300 of 29,201 recalls

Medical DeviceSeptember 10, 2019· Alto Development Corp

Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1200-08. For Recalled...

The Issue: Some Thorecon disposable tensioners supplied in different Plating System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Alto Development Corp

Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1500-04-S. For...

The Issue: Some Thorecon disposable tensioners supplied in different Plating System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Alto Development Corp

Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1300-04-S. For...

The Issue: Some Thorecon disposable tensioners supplied in different Plating System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a /1000g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a /1000g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a / 980g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Exactech, Inc.

Recalled Item: Ergo 3.2mm K-wire - Product Usage: The devices is used Recalled by Exactech,...

The Issue: Potential for the wire to fracture at the threads and remain in the glenoid.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a /980g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2019· Medline Industries Inc

Recalled Item: MEDLINE ELECTRIC SURGICAL CLIPPER AND BASE Recalled by Medline Industries...

The Issue: The recall is being conducted due to a potential defective component on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2019· CooperSurgical, Inc.

Recalled Item: Embryology Heated Plate within the RI Witness Recalled by CooperSurgical,...

The Issue: The touchpad may not work properly after cleaning.

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

Class III — Low RiskOngoing
Medical DeviceSeptember 4, 2019· Beckman Coulter Inc.

Recalled Item: Synchron Systems Opiate 2000 ng Reagent (OP2 1 x 250) Recalled by Beckman...

The Issue: Cross-reactivity testing may not meet the claims indicated in the Opiate...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2019· Beckman Coulter Inc.

Recalled Item: Opiate 300 Ng Reagent (OP 1 X 250) for use Recalled by Beckman Coulter Inc....

The Issue: Cross-reactivity testing may not meet the claims indicated in the Opiate 300...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2019· Elekta Inc

Recalled Item: Monaco RTP System Recalled by Elekta Inc Due to It is possible that the...

The Issue: It is possible that the forced electron density settings will be changed for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2019· Elekta Inc

Recalled Item: Monaco RTP System Recalled by Elekta Inc Due to It is possible that the...

The Issue: It is possible that the forced electron density settings will be changed for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2019· GE Healthcare, LLC

Recalled Item: Achilles Express Bone Sonometer Recalled by GE Healthcare, LLC Due to...

The Issue: Certain Achilles Express and Achilles Insight systems were shipped with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2019· GE Healthcare, LLC

Recalled Item: Achilles Insight Bone Sonometer Recalled by GE Healthcare, LLC Due to...

The Issue: Certain Achilles Express and Achilles Insight systems were shipped with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· Spacelabs Healthcare, Inc.

Recalled Item: Xhibit Central Recalled by Spacelabs Healthcare, Inc. Due to The firm...

The Issue: The firm received reports of loss of audio alarm after a power failure or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· Philips Ultrasound Inc

Recalled Item: Transducer S8-3t UDI (01)00884838073524 Can be used as Recalled by Philips...

The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· Philips Ultrasound Inc

Recalled Item: Transducer S7-3t UDI (01)00884838061439 Can be used with: Recalled by...

The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· Philips Ultrasound Inc

Recalled Item: Transducer S8-3t UDI (01)00884838067523 Can be used with: Recalled by...

The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...

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

Class II — Potential Health HazardOngoing