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. 2,487 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,487 in last 12 months

Showing 3402134040 of 51,202 recalls

Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: Spike Set Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker AutoPlex System. Model Numbers 0607-687-000 Recalled by Stryker...

The Issue: The Piston Head can become separated from the Delivery Piston, blocking the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-022F with 0.22 micron filter and FP Clip. Packaged in a Tyvek pouch...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T095-120 IV Set with 1.2 Micron Filter. Packaged in a Tyvek pouch Recalled...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-000F Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T090-022V 90" 20 Drop IV Admin Set Needle free Y-Site Recalled by WalkMed...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: The pump (with cushioning foam inserts) is packaged in a Recalled by WalkMed...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of the Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: The pump (with cushioning foam inserts) is packaged in a Recalled by WalkMed...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of the Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T105-000WC IV Set w/2 Y-Sites Recalled by WalkMed Infusion, LLC Due to...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T090-000 90" 20 Drop IV Admin Set. Packaged in a Tyvek pouch Recalled by...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2016· Cardiovascular Systems Inc

Recalled Item: ViperWire Advance Peripheral Guide Wire Recalled by Cardiovascular Systems...

The Issue: The pouch label was missing the use by date (UBD) of 2018-04.

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

Class II — Potential Health HazardOngoing
FoodJune 13, 2016· Kellogg Company

Recalled Item: Kellogg's Special K Mini Brownies Fudge Recalled by Kellogg Company Due to...

The Issue: Kellogg Company initiated a voluntary recall of multiple snack food items...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2016· Kellogg Company

Recalled Item: Keebler Animals Crackers Recalled by Kellogg Company Due to Undeclared Allergen

The Issue: Kellogg Company initiated a voluntary recall of multiple snack food items...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2016· Kellogg Company

Recalled Item: Keebler Gripz Chips D 325 ct Bulk Recalled by Kellogg Company Due to...

The Issue: Kellogg Company initiated a voluntary recall of multiple snack food items...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2016· Kellogg Company

Recalled Item: Premium Whole Chocolate Cremes 25 lb Recalled by Kellogg Company Due to...

The Issue: Kellogg Company initiated a voluntary recall of multiple snack food items...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2016· Kellogg Company

Recalled Item: Famous Amos Cookies Chocolate Chip Pecan Recalled by Kellogg Company Due to...

The Issue: Kellogg Company initiated a voluntary recall of multiple snack food items...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2016· National Frozen Foods Corporation

Recalled Item: Not Ready to Eat Recalled by National Frozen Foods Corporation Due to...

The Issue: Not Ready To Eat IQF Sysco Classic Peas & Onions are recalled because they...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2016· National Frozen Foods Corporation

Recalled Item: Not Ready to Eat Recalled by National Frozen Foods Corporation Due to...

The Issue: Not Ready To Eat IQF Mixed Vegetables are recalled because they have a...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2016· Kellogg Company

Recalled Item: Keebler 5 Flavor Mod Recalled by Kellogg Company Due to Undeclared Allergen

The Issue: Kellogg Company initiated a voluntary recall of multiple snack food items...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2016· Kellogg Company

Recalled Item: Kellogg's Special K Mini Brownies Blondie Recalled by Kellogg Company Due to...

The Issue: Kellogg Company initiated a voluntary recall of multiple snack food items...

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

Class II — Potential Health HazardOngoing
Refund