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. 2,700 recalls have been distributed to Louisiana in the last 12 months.
Showing 4321–4340 of 51,202 recalls
Recalled Item: Katy's KITCHEN Originals LEMON GELATIN MIX MEXCLA DE GELATINA DE LIMON...
The Issue: After an investigation, the firm discovered that a sifter used in the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cisplatin Injection Recalled by ACCORD HEALTHCARE, INC. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDLINE MAXORB EXTRA ALGINATE WOUND DRESSING 4X4 SQUARE Recalled by Advanced...
The Issue: Due to defects on primary packaging pouch that compromise the device's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hollister CalciCare Calcium Alginate Dressing calcium alginate dressings...
The Issue: Due to defects on primary packaging pouch that compromise the device's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Calcium Alginate Dressing MFR# 3562 Wound dressing indicated for...
The Issue: Due to defects on primary packaging pouch that compromise the device's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin@home Transmitter The Merlin@home" (M@h) transmitter is intended...
The Issue: Due to heart transmitter not being able to upgrade to the current software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin@home with the MerlinOnDemand capability Transmitter Merlin@home with...
The Issue: Due to heart transmitter not being able to upgrade to the current software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ascorbic Acid Inj. Solution Recalled by Staska Pharmaceuticals, Inc. Due to...
The Issue: Presence of Particulate Matter: Presence of glass particulates.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ciclopirox Gel 0.77% Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: Defective Container: Firm received complaints of broken tube at the seal.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Z-800 Infusion System Product Name: Z-800WF Model/Catalog...
The Issue: For the Z-800WF pumps, the WiFi software was not compatible with the pump...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT...
The Issue: Disposable biopsy instruments were potentially manufactured missing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 PSA assay Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: The IMMULITE 2000 PSA assay for use on the IMMULITE 2000 and IMMULITE 2000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Great Value Diced Peaches Recalled by Walmart Inc Due to FD&C Red No 3 was...
The Issue: FD&C Red No 3 was not declared as an ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Great Value Cherry Mixed Fruit Recalled by Walmart Inc Due to FD&C Red No 3...
The Issue: FD&C Red No 3 was not declared as an ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AMBU / KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.