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. 1,819 recalls have been distributed to Florida in the last 12 months.
Showing 51041–51060 of 55,837 recalls
Recalled Item: Pinnacle¿ Destination¿ Peripheral Guiding Sheath Recalled by Terumo Medical...
The Issue: Medical devices were incorrectly labeled with extended expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Glidesheath (tm) Recalled by Terumo Medical Corporation Due to...
The Issue: Medical devices were incorrectly labeled with extended expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******QTY 1***APEX Arthroscopy Tubing Set. Intended for use for Recalled by...
The Issue: Conmed Linvatec received complaints that their products C7120 APEX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Articulated Driver A nonpowered hand-held device intended for...
The Issue: When torque is applied to the Articulated Driver at the maximum angle, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TotalCare Bed used with AccuMax Quantum VPC mattress AccuMax Quantum...
The Issue: When the bed is put into the chair egress position, the magnets on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Oasys Midline Occiput Plate-1) Small 2) Medium 3) Large Recalled by...
The Issue: Stryker has received reports from customers indicating post-operative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEO-MED ORTHO TOTAL JOINT TRACECART(R) Recalled by DeRoyal Industries Inc...
The Issue: DeRoyal recalled kits that contained Stryker togas which were recalled for a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******APEX Arthroscopy Tubing Set. Intended for use for joint Recalled by...
The Issue: Conmed Linvatec received complaints that their products C7120 APEX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pharmalucence Kit for the Preparation of Technetium Tc 99m Sestamibi...
The Issue: Presence of Particulate Matter; particulate found in retain samples
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefazolin Recalled by Sandoz Incorporated Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Sandoz Inc is recalling Cefazolin for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fudge Buttercream Frosted Peanut Butter cookies Recalled by Cheryls Due to...
The Issue: Undeclared allergen due to use of incorrect packaging on peanut butter cookies.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lightlife Farmer's Market Veggie Burgers Recalled by Conagra Inc Due to The...
The Issue: The product packaging for Lighthouse Farmer's Market Veggie Burgers may...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: R3 (TM) XLPE ACETABULAR LINER UHMWPE Recalled by Smith & Nephew Inc Due to...
The Issue: One batch of 60 mm 20o R3 XLPE liner may be laser etched and packaged as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens MEVATRON series Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: The information regarding the FILM Mode calibration may have been considered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3 (TM) XLPE ACETABULAR LINER UHMWPE Recalled by Smith & Nephew Inc Due to...
The Issue: One batch of 60 mm 20o R3 XLPE liner may be laser etched and packaged as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guanabenz 8 mg/ml Injection Recalled by Lowlite Investments, Inc. D/B/A...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adenosine-Mono-Phosphate Injection Recalled by Lowlite Investments, Inc....
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cal-Phos 1000 Injection Recalled by Lowlite Investments, Inc. D/B/A Olympia...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phentolamine 20 mg/ml Injection Recalled by Lowlite Investments, Inc. D/B/A...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diphenhydramine 50 mg/ml Injection Recalled by Lowlite Investments, Inc....
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.