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. 2,670 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,670 in last 12 months

Showing 3744137460 of 55,837 recalls

FoodMay 4, 2016· Ohio Hickory Harvest Brand Products Inc.

Recalled Item: Big Y cranberry nut trail mix in plastic tub NET Recalled by Ohio Hickory...

The Issue: The firm was notified by their supplier that the products may be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 4, 2016· Ohio Hickory Harvest Brand Products Inc.

Recalled Item: Hickory Harvest FOODS Rucker's Cajun Mix 25 lb. bag in Recalled by Ohio...

The Issue: The firm was notified by their supplier that the products may be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 4, 2016· Ohio Hickory Harvest Brand Products Inc.

Recalled Item: Roasted No Salt Sunflower Kernel s under the following brand Recalled by...

The Issue: The firm was notified by their supplier that the products may be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 4, 2016· Sandridge Food Corporation

Recalled Item: Crunchy Wheatberry Salad Kit 12.75 LB (5.78kg) ***SUNFLOWER SEED POUCH:...

The Issue: The firm was notified by their supplier that the product may be contaminated...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 4, 2016· Ohio Hickory Harvest Brand Products Inc.

Recalled Item: Roasted & Salted Sunflower Kernels under the following brand names: Recalled...

The Issue: The firm was notified by their supplier that the products may be...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 4, 2016· Fresenius Kabi USA, LLC

Recalled Item: OCTREOTIDE ACETATE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Failed Impuities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2016· Fresenius Kabi USA, LLC

Recalled Item: OCTREOTIDE ACETATE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Failed Impuities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Zimmer Plates and Screws (ZPS) 4.0 mm Cancellous Screw Fully Threaded...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Zimmer Plates and Screws (ZPS) 2.7 mm Cortical Screw SelfTapping Recalled by...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: ITST intertrochanteric/subtrochanteric fixation 4.5 mm diameter cortical...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Herbert Cannulated Bone Screw System Recalled by Zimmer Manufacturing B.V....

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Cordis Corporation

Recalled Item: Cordis PRECISE (R) PRO RX Nitinol Stent System (Carotid) Recalled by Cordis...

The Issue: Inability to deploy the stent or partial stent deployment.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Trilogy self-tapping bone screw Bone screw 4.5x25 selftap 00625004525 Bone...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: M/DN Intramedullary Fixation 4.2 mm Diameter Cortical Screw Recalled by...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: VersaFx Femoral Fixation System Hex head compression screw 4.7 mm Recalled...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Zimmer universal locking system (ULS) 3.5 mm cortical screw selftapping...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Hgp ii acetabular cup bone screw selftap 6.5x15mm 00662406515 Hgp Recalled...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Mini MagnaFx Cannulated Screw Fixation System Small Cannulated Bone Screw...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Cordis Corporation

Recalled Item: Cordis PRECISE (R) RX Nitinol Stent System (Biliary) Recalled by Cordis...

The Issue: Inability to deploy the stent or partial stent deployment.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Periarticular plating system Recalled by Zimmer Manufacturing B.V. Due to A...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing