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. 875 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
875 in last 12 months

Showing 52341–52360 of 55,837 recalls

FoodMarch 14, 2013· F.H.G Corporation dba Integrity Nutraceuticals

Recalled Item: MUSCLEPHARM brand COMBAT POWDER (R) Recalled by F.H.G Corporation dba...

The Issue: One lot of each product may have extraneous materials due to a problem on...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 13, 2013· New Chapter, Inc.

Recalled Item: NewChapter Probiotic Elderberry Recalled by New Chapter, Inc. Due to...

The Issue: The product may contain an undeclared allergen soy

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 13, 2013· Daesang America Inc

Recalled Item: Sunchang Ssamjang Sesame and Garlic Seasoned Bean Paste 500 g Recalled by...

The Issue: Sesame and Garlic Flavored Mixed Soy Bean Paste contains peanut powder which...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 13, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Vitamin D Assay (500 tests) Recalled by Siemens Healthcare...

The Issue: Negative bias in patient samples for Vitamin D

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Archer 0.035 inch (0.89mm) Super Stiff Guidewire Recalled by...

The Issue: Medtronic has identified an issue involving specific lot numbers of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Archer Super Stiff Guidewire 0.035 inch (0.89mm) Recalled by...

The Issue: Medtronic has identified an issue with a specific lot of the Archer 0.035...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Vitamin D Assay (100 tests) Recalled by Siemens Healthcare...

The Issue: Negative bias in patient samples for Vitamin D

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Vitamin D Calibrator 2-pack Recalled by Siemens Healthcare...

The Issue: Negative bias in patient samples for Vitamin D

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Separation Technology, Inc.

Recalled Item: SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE. Produce a monolayer of cells...

The Issue: Separation Technology, Inc. recalled SlidePrep Plus Cytology Centrifuges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Vitamin D Calibrator 6-pack Recalled by Siemens Healthcare...

The Issue: Negative bias in patient samples for Vitamin D

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Epocal

Recalled Item: epoc BGEM Test Card (Catalogue number CT-1004-00-00). quantitative testing...

The Issue: This recall is being initiated because the affected lots of this product may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Masimo Corporation

Recalled Item: Rad-8 Pulse Oximeters The Rad-8 family of pulse oximeters and Recalled by...

The Issue: Masimo has identified a very small number (0.02%) of Rad-8 devices with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2013· GE Healthcare It

Recalled Item: The Centricity Laboratory System is intended to be an information Recalled...

The Issue: GE Healthcare has become aware of a potential safety issue associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT 16-Slice Water Recalled by Philips Medical Systems (Cleveland)...

The Issue: Philips Healthcare received a report from the field stating when they viewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2013· Custom Ultrasonics, Inc.

Recalled Item: Custom Ultrasonics System 83 Plus 2 and Plus 9 Endoscope Washer/Disinfector....

The Issue: Certain System 83 Plus 2 and System 83 Plus 9 units running the Windows 7...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2013· Berchtold Corp.

Recalled Item: Hand Controls for Operon D750 Recalled by Berchtold Corp. Due to The firm...

The Issue: The firm received complaints for unintended movements.

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

Class II — Potential Health HazardOngoing
FoodMarch 12, 2013· Purely American, Inc.

Recalled Item: ADIRONDACK GETAWAY PASTA TOSS MIX 11oz cello bag Contents: All Recalled by...

The Issue: The firm was notified by the Ohio Department of Agriculture that several of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 12, 2013· Purely American, Inc.

Recalled Item: Pasta Salad Mix Recalled by Purely American, Inc. Due to The firm was...

The Issue: The firm was notified by the Ohio Department of Agriculture that several of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 12, 2013· Purely American, Inc.

Recalled Item: MAMA MARINO'S MINESTRONE SOUP MIX 15 oz cello bag Contents: Recalled by...

The Issue: The firm was notified by the Ohio Department of Agriculture that several of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 12, 2013· Purely American, Inc.

Recalled Item: MARIN COUNTY CARROT CAKE MIX 18.5 oz coffee bag Contents: Unbleached white...

The Issue: The firm was notified by the Ohio Department of Agriculture that several of...

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

Class II — Potential Health HazardOngoing
Refund