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. 2,534 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,534 in last 12 months

Showing 2132121340 of 29,201 recalls

Medical DeviceJanuary 29, 2016· Verathon, Inc.

Recalled Item: GlideScope Titanium Single-Use Video Laryngoscope. It is a single-use video...

The Issue: The firm has become aware of the potential for disruption (flickering) in...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 29, 2016· Corin USA Limited

Recalled Item: Trinity Acetabular Shell Product Usage: Total Hip Replacement. Recalled by...

The Issue: Potential for abrasion of the sterile barrier pouches of the new packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2016· Valeant Pharmacueticals International

Recalled Item: Orapharma (Onpharma) Onset Mixing Pen Rx only Recalled by Valeant...

The Issue: It has been determined that the Onset Mixing Pen has an optimal use period...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2016· Corin USA Limited

Recalled Item: Trinity Acetabular Shell Product Usage Total Hip Replacement. Recalled by...

The Issue: Potential for abrasion of the sterile barrier pouches of the new packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2016· Biomet, Inc.

Recalled Item: Crosslock DVR ePAK -Sterile Recalled by Biomet, Inc. Due to Foreign Object...

The Issue: Components of the DVR ePAKs can oxidize during shipment and storage prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2016· Novadaq Technologies Inc.

Recalled Item: PINPOINT Endoscopic Fluorescence Imaging System Recalled by Novadaq...

The Issue: It has been determined that the PINPOINT Operator's Manual does not contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2016· Corin USA Limited

Recalled Item: Trinity Acetabular System Product Usage - Total Hip Replacement. Recalled by...

The Issue: Potential for abrasion of the sterile barrier pouches of the new packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2016· Cook Inc.

Recalled Item: Ascend¿ AQ¿ Ureteral Dilation Balloon Catheter Set The Ascend¿ AQ¿ Recalled...

The Issue: Cook Medical is voluntarily recalling specific lots of the Ultraxx"...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2016· Physio-Control, Inc.

Recalled Item: LIFEPAK15 monitor/defibrillator with End-Tidal C02 (EtC02) feature...

The Issue: The firm became aware that when using EtC02 in the kPa or % setting and in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2016· Cook Inc.

Recalled Item: UltraxxTM Nephrostomy Balloon Set The Ultraxx" Nephrostomy Balloon Set...

The Issue: Cook Medical is voluntarily recalling specific lots of the Ultraxx"...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Syngo Dynamics-a Picture Archiving and Communication System (PACS)...

The Issue: Siemens' conducting a recall due to a potential issue when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2016· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FMC7 FITC: Model 430918. FMC7 is intended for in Recalled by Becton,...

The Issue: Becton, Dickinson and Company (BD) has determined that the FMC7 FITC (ASR)...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover P400 PREM U/M 18FR SIL FLY Item Code: Recalled by Covidien...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover PRECSION PRM 16FR SIL FLY Item Code: PP16SD Recalled by...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover P400 PREM U/M 18FR SIL COUDE CATH SECURE Recalled by Covidien...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover 4.5OZ MIDSTREAM W/CASTILE TOWL Item Code: 24015 Castile...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover PREM U/M 14FR SIL FLY Item Code: P4P14SD Recalled by Covidien...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover PREM U/M 14FR SLVR FLY Item Code: P4P14XSD Recalled by...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover P400 PREM UM 16FR SILV TMP CSD Item Recalled by Covidien LLC...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover KIT/STERILE PRESERVE CULT Item Code: 8000SA Castile soap...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing