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. 2,911 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,911 in last 12 months

Showing 63016320 of 55,837 recalls

DrugApril 24, 2024· SOMERSET THERAPEUTICS LLC

Recalled Item: Haloperidol decanoate Injection 50mg/mL Recalled by SOMERSET THERAPEUTICS...

The Issue: Presence of Foreign Substance: This oil based product may contain trace...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2024· Lupin Pharmaceuticals Inc.

Recalled Item: Cefdinir for Oral Suspension USP 250 mg/5 mL (60 mL when reconstituted)...

The Issue: Presence of foreign substance: Product complaint of foreign material in...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2024· Lupin Pharmaceuticals Inc.

Recalled Item: Cefdinir for Oral Suspension USP 125 mg/5 mL (60 mL when reconstituted)...

The Issue: Presence of foreign substance: Product complaint of foreign material in...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2024· Aurobindo Pharma USA Inc.

Recalled Item: Clorazepate Dipotassium Tablets Recalled by Aurobindo Pharma USA Inc. Due to...

The Issue: Discoloration: Dotted and yellow spots on tablets

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2024· Aurobindo Pharma USA Inc.

Recalled Item: Clorazepate Dipotassium Tablets Recalled by Aurobindo Pharma USA Inc. Due to...

The Issue: Discoloration: Dotted and yellow spots on tablets

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2024· Acella Pharmaceuticals, LLC

Recalled Item: Sodium Sulfacetamide 10% - Sulfur 5% Cleanser Recalled by Acella...

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 24, 2024· Barco N.V.

Recalled Item: MNA-420 ENC HDMI Recalled by Barco N.V. Due to We have identified a...

The Issue: We have identified a potential issue with the SFP+ module supplied by Molex...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2024· Olympus Corporation of the Americas

Recalled Item: EasySuite 4K Integrated Operating Room System Model/Catalog Number:...

The Issue: A subset of the ES4K systems do not have complete records for earth leakage...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2024· Lucid Diagnostics, Inc.

Recalled Item: Brand Name: EsophaCap Product Name: EsophaCap (25mm diameter Recalled by...

The Issue: The EsophaCap sponge may be at increased risk of detaching from the string...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2024· Lucid Diagnostics, Inc.

Recalled Item: Brand Name: EsophaCap Product Name: EsophaCap (20mm diameter Recalled by...

The Issue: The EsophaCap sponge may be at increased risk of detaching from the string...

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

Class II — Potential Health HazardOngoing
DrugApril 23, 2024· Regeneron Pharmaceuticals Inc

Recalled Item: EYLEA Recalled by Regeneron Pharmaceuticals Inc Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Complaints of syringe breakage

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 23, 2024· EPI Health, LLC

Recalled Item: minolira (minocycline hydrochloride) extended-release tablets Recalled by...

The Issue: CGMP Deviation: Discontinuation of the Quality program by manufacturer that...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 23, 2024· EPI Health, LLC

Recalled Item: Cloderm (clocortolone pivalate) Cream Recalled by EPI Health, LLC Due to...

The Issue: CGMP Deviation: Discontinuation of the Quality program by manufacturer that...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 23, 2024· EPI Health, LLC

Recalled Item: minolira (minocycline hydrochloride) extended-release tablets Recalled by...

The Issue: CGMP Deviation: Discontinuation of the Quality program by manufacturer that...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 23, 2024· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Coviden Monoject 60ml Syringe Luer-Lock Tip-used to inject fluid into...

The Issue: Quarantined product was inadvertently distributed

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2024· Stryker Neurovascular

Recalled Item: Trevo ProVue Recalled by Stryker Neurovascular Due to Neurovascular devices...

The Issue: Neurovascular devices did not meet the minimum sample size required for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2024· Stryker Neurovascular

Recalled Item: Trevo Trak 21 Microcatheter Recalled by Stryker Neurovascular Due to...

The Issue: Neurovascular devices did not meet the minimum sample size required for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2024· Stryker Neurovascular

Recalled Item: Synchro .014"guide wire Recalled by Stryker Neurovascular Due to...

The Issue: Neurovascular devices did not meet the minimum sample size required for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2024· Stryker Neurovascular

Recalled Item: DAC 044 115cm Recalled by Stryker Neurovascular Due to Neurovascular devices...

The Issue: Neurovascular devices did not meet the minimum sample size required for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2024· Stryker Neurovascular

Recalled Item: Trevo NXT ProVue 3 x 32 Recalled by Stryker Neurovascular Due to...

The Issue: Neurovascular devices did not meet the minimum sample size required for...

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

Class II — Potential Health HazardOngoing