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. 2,865 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,865 in last 12 months

Showing 1408114100 of 55,837 recalls

Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...

The Issue: Upgraded software version makes an automatic change in laser configuration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on syngo.via Recalled by...

The Issue: Upgraded software version makes an automatic change in laser configuration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...

The Issue: Upgraded software version makes an automatic change in laser configuration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...

The Issue: Upgraded software version makes an automatic change in laser configuration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS SOMATOM with software syngo CT VA30A_SP4 Models: SOMATOM go.Now...

The Issue: Software error may result in sporadic problems causing scanning workflow...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: YSIO X.Pree Recalled by Siemens Medical Solutions USA, Inc Due to For the...

The Issue: For the automated multi-image-acquisition procedure Ortho x-ray collimation...

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

Class II — Potential Health HazardOngoing
DrugMarch 4, 2022· Direct Rx

Recalled Item: Alprazolam C-IV 2 mg Recalled by Direct Rx Due to CGMP Deviations: The...

The Issue: CGMP Deviations: The Recall is due to the potential cross-contamination at...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2022· Fagron, Inc

Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2022· Fagron, Inc

Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2022· Fagron, Inc

Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2022· Fagron, Inc

Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2022· Fagron, Inc

Recalled Item: SyrSpend SF Suspending Base Recalled by Fagron, Inc Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Product: Product is contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 4, 2022· Fagron, Inc

Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2022· Fresenius Kabi USA, LLC

Recalled Item: Sodium Acetate Injection Recalled by Fresenius Kabi USA, LLC Due to Presence...

The Issue: Presence of particulate matter: particulates composed of carbon and oxygen...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 4, 2022· Direct Rx

Recalled Item: Alprazolam C-IV 1 mg 60-count bottles Recalled by Direct Rx Due to CGMP...

The Issue: CGMP Deviations: The Recall is due to the potential cross-contamination at...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 4, 2022· Swanson Health Products, Inc

Recalled Item: Swanson Ultra: Vitamin B12 Methylcobalamin High Absorption 60 serving per...

The Issue: Dietary supplement may contain potential metal shavings greater than or...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 4, 2022· SML Distribution, LLC

Recalled Item: Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold)...

The Issue: The product was distributed without FDA authorization or clearance for...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 4, 2022· Draegar Medical Systems, Inc.

Recalled Item: Drager Infinity CentralStation Software versions VG2.1.2 and VG2.1.2 SU12....

The Issue: Software issue resulting in temporary loss of central monitoring functionality.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2022· GE Healthcare, LLC

Recalled Item: GE Healthcare MR Systems Recalled by GE Healthcare, LLC Due to During the...

The Issue: During the de-installation of an MR system magnet, if all rigging and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2022· WHPM Inc.

Recalled Item: First SIGN SARS-CoV-2 Antigen Test Recalled by WHPM Inc. Due to Frm became...

The Issue: Frm became aware that a customer complaint was reported to US FDA that...

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

Class II — Potential Health HazardOngoing