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. 1,921 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,921 in last 12 months

Showing 3212132140 of 55,837 recalls

FoodJune 7, 2017· Lyrical Foods Inc

Recalled Item: Kite Hill Almond Yogurt Recalled by Lyrical Foods Inc Due to Lyrical Foods...

The Issue: Lyrical Foods is voluntarily recalling four flavors of Kite Hill Almond...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 (Model No. 728323) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: IQon Spectral CT (Model No. 728332) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core (Model No. 728321) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT (Model No. 728306) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance Big Bore Radiology CT (Model No. 728244) software version...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT (Model No. 728326) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance Big Bore Oncology CT (Model No. 728243) software version Recalled...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT SP (Model No. 728311 Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 (Model No. 728231) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
FoodJune 6, 2017· Morris J. Golombeck, Inc.

Recalled Item: BIRDS EYE CHILIES MJG # 8178 Recalled by Morris J. Golombeck, Inc. Due to...

The Issue: Product may contain peanuts

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 6, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Axiom Artis Recalled by Siemens Medical Solutions USA, Inc Due to Potential...

The Issue: Potential for liquid entry

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q and Q.Zen Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for liquid entry

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Zee and Zeego Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for liquid entry

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Spectranetics Corporation

Recalled Item: Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid...

The Issue: Potential for flouroscopially visible marker band at the tip of the Rapid...

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

Class II — Potential Health HazardOngoing
DrugJune 6, 2017· Bausch & Lomb, Inc.

Recalled Item: NasalCrom (cromolyn sodium) Nasal Spray Recalled by Bausch & Lomb, Inc. Due...

The Issue: CGMP Deviations: Possibility of the presence of microbial contamination in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 6, 2017· Microbiologics Inc

Recalled Item: Microbiologics QC Sets and Panels. BD MAX" CT/GC/TV Verification and...

The Issue: Real-time shelf life testing failed at 24 months

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Microbiologics Inc

Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...

The Issue: Real-time shelf life testing failed at 24 months

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Microbiologics Inc

Recalled Item: Microbiologics QC Sets and Panels: Helix Elite. Extended Enteric Bacterial...

The Issue: Real-time shelf life testing failed at 24 months

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Microbiologics Inc

Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...

The Issue: Real-time shelf life testing failed at 24 months

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

Class II — Potential Health HazardOngoing