Product Recalls in Florida

Product recalls affecting Florida — including food, drugs, consumer products, medical devices, and vehicles distributed to Florida. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,723 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,723 in last 12 months

Showing 2602126040 of 55,837 recalls

DrugOctober 29, 2018· Sciegen Pharmaceuticals Inc

Recalled Item: GSMS Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due to CGMP...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Sciegen Pharmaceuticals Inc

Recalled Item: Westminister Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Sciegen Pharmaceuticals Inc

Recalled Item: Westminister Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Sciegen Pharmaceuticals Inc

Recalled Item: GSMS Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due to CGMP...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Sciegen Pharmaceuticals Inc

Recalled Item: Westminister Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Westminster Pharmaceuticals Llc

Recalled Item: Westminster Irbesartan Tablets Recalled by Westminster Pharmaceuticals Llc...

The Issue: CGMP Deviations: FDA laboratory testing confirmed traces of NDEA impurity in...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Westminster Pharmaceuticals Llc

Recalled Item: Westminster Irbesartan Tablets Recalled by Westminster Pharmaceuticals Llc...

The Issue: CGMP Deviations: FDA laboratory testing confirmed traces of NDEA impurity in...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Westminster Pharmaceuticals Llc

Recalled Item: Westminster Irbesartan Tablets Recalled by Westminster Pharmaceuticals Llc...

The Issue: CGMP Deviations: FDA laboratory testing confirmed traces of NDEA impurity in...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 29, 2018· J&J Snack Foods Handheld Corp

Recalled Item: Fit & Active Southwest Veggie Stuffed Sandwiches NET WT 9 Recalled by J&J...

The Issue: The firm was notified by their supplier that the vegetables used in the...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 28, 2018· Feast Mode Blending & Filling

Recalled Item: Feast Mode Flavors Garlic Beer Seasoning Recalled by Feast Mode Blending &...

The Issue: Feast Mode Garlic Beer Seasoning is mislabeled as "Gluten Free"

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 26, 2018· Maribel's Sweets, Inc.

Recalled Item: Cacao Market by MarieBelle Orange Peels 60% Dark Chocolate Bar Recalled by...

The Issue: Product contains undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 26, 2018· Maribel's Sweets, Inc.

Recalled Item: MarieBelle brand Japanese Matcha Japanese Green Tea and White Chocolate Bar...

The Issue: Product contains undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 26, 2018· Maribel's Sweets, Inc.

Recalled Item: Cacao Market by MarieBelle Rosemary Truffle Salt 60% Dark Chocolate Bar...

The Issue: Product contains undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 26, 2018· Implant Direct Sybron Manufacturing, LLC

Recalled Item: Implant Direct Recalled by Implant Direct Sybron Manufacturing, LLC Due to...

The Issue: packaging error; An internal QA inspection revealed that a incorrect healing...

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

Class II — Potential Health HazardOngoing
DrugOctober 26, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Levetiracetam in 0.54 % Sodium Chloride Injection 1 Recalled by Dr. Reddy's...

The Issue: Labeling: Label Error on Declared Strength; the pre-printed text on the...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 25, 2018· Valley Processing Inc.

Recalled Item: Apple juice concentrate and organic apple juice concentrate in 52 gallon...

The Issue: The apple juice concentrates contain high levels of inorganic arsenic. The...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 25, 2018· Intuitive Surgical, Inc.

Recalled Item: da Vinci SP Instrument Arm Drape. QTY 1 Pouch Recalled by Intuitive...

The Issue: The instrument drape may tear while draping the Patient Side Cart presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2018· Maquet Cardiovascular Us Sales, Llc

Recalled Item: QUADROX-i Neonatal with integrated arterial filter and VHK 11000 (VKMO...

The Issue: There is a potential for blood leakage at the blood inlet connector when...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 25, 2018· Maquet Cardiovascular Us Sales, Llc

Recalled Item: QUADROX-i Neonatal without integrated arterial filter and VHK 11000 (VKMO...

The Issue: There is a potential for blood leakage at the blood inlet connector when...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2018· Zimmer Biomet, Inc.

Recalled Item: Biomet 20mm Compress Device Short Anchor Plug With Drill Set Recalled by...

The Issue: Potential metal burrs in the holes of the device preventing the appropriate...

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

Class II — Potential Health HazardOngoing