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 2498125000 of 51,202 recalls

Medical DeviceAugust 8, 2018· Helena Laboratories, Corp.

Recalled Item: ColoCARE Recalled by Helena Laboratories, Corp. Due to The positive control...

The Issue: The positive control on some tests of the lots did not appropriately react...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Implant Direct Sybron Manufacturing, LLC

Recalled Item: ImplantDirect Legacy 3 Implant Recalled by Implant Direct Sybron...

The Issue: Two units in distribution were found to be mislabeled on the vial cap with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Helena Laboratories, Corp.

Recalled Item: ColoCARE Recalled by Helena Laboratories, Corp. Due to The positive control...

The Issue: The positive control on some tests of the lots did not appropriately react...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2018· Medtronic Inc.

Recalled Item: Minimed Model 503 Remote Transmitter (MMT-503 Recalled by Medtronic Inc. Due...

The Issue: There is a potential security vulnerability related to the use of the remote...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 7, 2018· Medtronic Inc.

Recalled Item: Minimed Model 500 Remote Control (MMT-500 Recalled by Medtronic Inc. Due to...

The Issue: There is a potential security vulnerability related to the use of the remote...

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

Class I — Serious Health HazardOngoing
DrugAugust 7, 2018· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Doxycycline Hyclate USP Tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due...

The Issue: Failed Dissolution Specifications: manufacturer West-Ward Pharm Corp....

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2018· Mylan Pharmaceuticals Inc.

Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: Out of specification test...

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

Class III — Low RiskOngoing
Refund
DrugAugust 7, 2018· Mylan Pharmaceuticals Inc.

Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: Out of specification test...

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

Class III — Low RiskOngoing
Refund
FoodAugust 7, 2018· Natures Bounty Inc

Recalled Item: BLUE GREEN ALGAE: Packaged under the following brands: AMERICAN HEALTH...

The Issue: High level of microcystin observed in the product.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodAugust 6, 2018· Country Favor Inc.

Recalled Item: BEST TASTE BRAND SNACK GINGER SLICED Recalled by Country Favor Inc. Due to...

The Issue: Product contains high levels of undeclared sulfites.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 6, 2018· Dannoritzer Medizintechnik GmbH & Co. KG

Recalled Item: Laparoscopy Instruments Instructions For Use (IFU) for the following:...

The Issue: The Manual cleaning process and the usability of the reprocessing...

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

Class III — Low RiskOngoing
Medical DeviceAugust 6, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Ysio MAX (model number 10762470) with Tube stand 3D V Recalled by Siemens...

The Issue: In rare cases of high clinical workload, the steel cables inside the lifting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Ysio (model number 10281013 or 10281163) with Tube stand 3D Recalled by...

The Issue: In rare cases of high clinical workload, the steel cables inside the lifting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Multix MT (model number 8395415 or 8395399 or 8395381) Recalled by...

The Issue: In rare cases of high clinical workload, the steel cables inside the lifting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2018· Agfa Healthcare NV

Recalled Item: Enterprise Imaging Desktops Enterprise Imaging Desktops (Radiology...

The Issue: Adding an additional comparison study to the Clinical Side Bar in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2018· Zimmer Biomet, Inc.

Recalled Item: Biomet Sports Medii cine Juggerknot Long Flex Drill Bit with Recalled by...

The Issue: Expiration date incorrectly listed on the label

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2018· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System Recalled by Elekta, Inc. Due to Order...

The Issue: Order Status Remains Approved When Should Indicate Complete.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Multix Fusion system is a radiographic system: Models: Multix Fusion...

The Issue: Steel cables inside the lifting column of the overhead tube, may rapture...

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

Class II — Potential Health HazardOngoing
FoodAugust 3, 2018· Hostess Brands, LLC

Recalled Item: Hostess Brownies Cookies 'n Cr¿me packaged in the following ways: Recalled...

The Issue: The product ingredients statement declares egg ingredients, but the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 3, 2018· Product Quest Manufacturing LLC

Recalled Item: DG health Recalled by Product Quest Manufacturing LLC Due to CGMP...

The Issue: CGMP Deviations: products manufactured under conditions that could impact...

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

Class II — Potential Health HazardOngoing
Refund