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. 1,132 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,132 in last 12 months

Showing 15261–15280 of 30,686 recalls

Medical DeviceFebruary 8, 2019· Terumo Medical Corporation

Recalled Item: Terumo Needle Recalled by Terumo Medical Corporation Due to There is a...

The Issue: There is a potential for a loss of package integrity that may compromise the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Draegar Medical Systems, Inc.

Recalled Item: Infinity Delta Family patient monitors The Infinity Delta Series...

The Issue: The firm is recalling their Delta family of patient monitors software due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Terumo Medical Corporation

Recalled Item: Terumo Sur-vet Needle Recalled by Terumo Medical Corporation Due to There is...

The Issue: There is a potential for a loss of package integrity that may compromise the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Terumo Medical Corporation

Recalled Item: Terumo Sur-vet Needle Recalled by Terumo Medical Corporation Due to There is...

The Issue: There is a potential for a loss of package integrity that may compromise the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Terumo Medical Corporation

Recalled Item: Terumo Sur-vet Needle Recalled by Terumo Medical Corporation Due to There is...

The Issue: There is a potential for a loss of package integrity that may compromise the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Canon Medical System, USA, INC.

Recalled Item: Infinix DP- i(Infinix-8000F) CAT-870B Catheterization Table (Titling) -...

The Issue: Table tilts without operator involvement as a result of liquid spilling into...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Riverpoint Medical, LLC

Recalled Item: Riverpoint Medical 18G Brachy Grid Recalled by Riverpoint Medical, LLC Due...

The Issue: The integrity of the sterile grid packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Cardiohelp Emergency Drive Recalled by Maquet Cardiovascular Us Sales, Llc...

The Issue: Upon servicing the gearwheel in the Emergency Drive the gearwheel may have...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 8, 2019· Terumo Medical Corporation

Recalled Item: Terumo Needle Recalled by Terumo Medical Corporation Due to There is a...

The Issue: There is a potential for a loss of package integrity that may compromise the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2019· Cordis Corporation

Recalled Item: Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: Recalled...

The Issue: Frayed pieces of the mounting card being inside the primary packaging.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 6, 2019· LW Scientific, Inc.

Recalled Item: LW Scientific ZIP IQ Combo Centrifuge Recalled by LW Scientific, Inc. Due to...

The Issue: The clear, plastic, polycarbonate hematocrit rotor may break apart during...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2019· LW Scientific, Inc.

Recalled Item: LW Scientific ZIP IQ Combo Centrifuge Recalled by LW Scientific, Inc. Due to...

The Issue: The clear, plastic, polycarbonate hematocrit rotor may break apart during...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2019· LW Scientific, Inc.

Recalled Item: LW Scientific ZIP IQ PCV Centrifuge Recalled by LW Scientific, Inc. Due to...

The Issue: The clear, plastic, polycarbonate hematocrit rotor may break apart during...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2019· Medica Corporation

Recalled Item: Medica Wash1-Wash solution used prior to Lipase assay on the Recalled by...

The Issue: Wash1 solution is ineffective in cleaning dispensing probe of TRIG and LDL...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2019· Abbott Ireland Diagnostics Division

Recalled Item: Abbott Alinity i Estradiol Reagent Kit - Product Usage: Alinity Recalled by...

The Issue: Patient results may be falsely elevated. This patient impact only applies to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2019· Abbott Ireland Diagnostics Division

Recalled Item: Abbott ARCHITECT Estradiol Reagent Kit - Product Usage: The ARCHITECT...

The Issue: Patient results may be falsely elevated. This patient impact only applies to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2019· CP Medical Inc

Recalled Item: Plain and Chromic Gut Absorbable Surgical Sutures Recalled by CP Medical Inc...

The Issue: Potential compromise of product sterility after routine monitoring for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2019· US Endoscopy Group Inc

Recalled Item: US Endoscopy Padlock Clip defect closure system The Recalled by US Endoscopy...

The Issue: Potential esophageal laceration during a patient procedure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2019· Encore Medical, Lp

Recalled Item: EMPOWR Locking Femoral Impactor Recalled by Encore Medical, Lp Due to The...

The Issue: The firm has received reports/complaints concerning the breakage of the tips...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2019· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: NexGenTrabecular Metal Tibial Half Block Augment Recalled by Zimmer...

The Issue: Potentially comingled, resulting in the product in the box potentially not...

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

Class II — Potential Health HazardOngoing