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 3816138180 of 55,837 recalls

Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Uniqcot 1/2" x 3" : 67-09 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Tonsil Sponges 1" Large : 50-01 Product Recalled by...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: Mass Eye & Ear Finger Cot Nasal 2's : Recalled by American Surgical Company...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· St Jude Medical Inc.

Recalled Item: Ellipse ICD (Implantable Cardioverter Defibrillator) Model CD2411-36Q...

The Issue: St. Jude Medical is recalling the Ellipse ICD (Implantable Cardioverter...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· Hologic, Inc

Recalled Item: CF InPlex ASR Card Recalled by Hologic, Inc Due to Complaints of false...

The Issue: Complaints of false positive HET mutations and leaking cards; could lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· Hologic, Inc

Recalled Item: Hologic InPlex CF Molecular Test (IVD) Recalled by Hologic, Inc Due to...

The Issue: Complaints of false positive HET mutations and leaking cards; could lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Trucount Absolute Counting Tubes: Model number: 340334 IVD Recalled by...

The Issue: One lot of lot of BD Trucount tubes may contain tubes from another lot....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· Shimadzu Medical Systems

Recalled Item: X-Ray Diagnostic Table Recalled by Shimadzu Medical Systems Due to Report of...

The Issue: Report of unintentional movement of table to reverse tilting.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· Biocare Medical, LLC

Recalled Item: Mach 4 Mouse Probe vial within the Mach 4 Universal HRP-Polymer Kit Recalled...

The Issue: Biocare Medical has identified a single lot (082715) of its Mach 4 HRP...

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

Class III — Low RiskOngoing
Medical DeviceMarch 30, 2016· Teleflex Medical

Recalled Item: Pleur-evac Chest Drainage System Recalled by Teleflex Medical Due to The...

The Issue: The label on the Tyvek bag is missing. This is used by customers to identify...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur CP Immunoassay System Recalled by Siemens Healthcare...

The Issue: The firm identified an issue in sample processing when using EZee-Nest...

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

Class III — Low RiskOngoing
FoodMarch 30, 2016· R.A.B. Food Group LLC

Recalled Item: Manischewitz Pistachio Orange Macaroons 10 oz. Distributed by: The...

The Issue: Manischewitz Pistachio Orange macaroons may contain pistachio shell fragments.

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

Class III — Low RiskOngoing
Refund
FoodMarch 30, 2016· Alimentos Congelados, S.A. (Pinula)

Recalled Item: Wylwood Fresh Frozen Broccoli Cuts Recalled by Alimentos Congelados, S.A....

The Issue: Alimentos Congelados, S.A. (Pinula) is voluntarily recalling 1,800 cases of...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 30, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Ondansetron Tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications; 12 month stability time point

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 29, 2016· Lee Seed Co Inc

Recalled Item: Yogurt Super Soynuts packaged in 16 oz. plastic bags and Recalled by Lee...

The Issue: Product contains undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 28, 2016· Philips Ultrasound, Inc.

Recalled Item: EPIQ DIAGNOSTIC ULTRASOUND SYSTEM Recalled by Philips Ultrasound, Inc. Due...

The Issue: The fasteners securing the control panel assembly to the base of the Philips...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Spacelabs Healthcare Inc

Recalled Item: The Spacelabs Healthcare Xhibit Telemetry Receiver (XTR) Recalled by...

The Issue: Reports of an abnormally high frequency of squelch events on Xhibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Becton Dickinson & Co.

Recalled Item: Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) Recalled by Becton...

The Issue: Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) // MacConkey II Agar...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific is voluntarily implementing a Medical Device Recall of one...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Stryker Endoscopy

Recalled Item: PneumoSure XL High Flow Insufflator and PneumoSure High Flow Insufflator...

The Issue: When operating the device in high flow mode (40L/min, 15 mmHg) and...

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

Class II — Potential Health HazardOngoing