Recalls affecting Florida
Notices that name Florida in their distribution area, plus every nationwide recall — nationwide recalls reach Florida too.
-
Class II · 7 months ago
Baxter Healthcare Corporation Brand Name: Welch Allyn recall: Display screen may unintentionally flicker due to a software issue. Exposure
Display screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in…
-
Class II · 7 months ago
Abbott Diagnostics Scarborough, Inc. Product Name: ID NOW" Influenza A & B 2 Model/ recall: It was confirmed that the impacted lot has a higher occurrence of invalid
It was confirmed that the impacted lot has a higher occurrence of invalid rates when compared to the product Instructions for Use.
-
Class II · 7 months ago
GE Medical Systems, LLC Centricity Universal Viewer Software Versions 5.0 SP6 through recall: There is a potential cybersecurity vulnerability affecting certain versions
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on…
-
Class II · 7 months ago
Hologic, Inc. Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/ recall: Due to product exhibiting potential to generate either invalid or false
Due to product exhibiting potential to generate either invalid or false negative results.
-
Class II · 7 months ago
Stryker Medical Division of Stryker Corporation Cub Pediatric Crib, Model FL19H recall: Cribs sold in the USA are missing two access door warning labels
Cribs sold in the USA are missing two access door warning labels.
-
Class II · 7 months ago
LeMaitre Vascular, Inc. Artegraft Vascular Graft recall: Labeling mix-up resulting in the incorrect lot outer packaging of product
Labeling mix-up resulting in the incorrect lot outer packaging of product.
-
Class II · 7 months ago
Convatec, EsteemBody Drainable Pouch REF:423653 10-35mm recall: Drainable large pouch may leak due to manufacturing issue
Drainable large pouch may leak due to manufacturing issue.
-
Class II · 7 months ago
Convatec, EsteemBody Drainable Pouch REF:423643, 10-45mm recall: Drainable large pouch may leak due to manufacturing issue
Drainable large pouch may leak due to manufacturing issue.
-
Class II · 7 months ago
Diagnostica Stago, Inc. Brand Name: STA Liatest D-Di Product Name: STA Liatest D-Di recall: After receiving customer complaints, investigations confirmed the presence
After receiving customer complaints, investigations confirmed the presence of a positive bias in D-Dimer measurements throughout the entire…
-
Class II · 7 months ago
GE Medical Systems, LLC Centricity Universal Viewer Software Versions 6.0 through 6.0 recall: There is a potential cybersecurity vulnerability affecting certain versions
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on…
-
Class II · 7 months ago
Elekta, Inc. Brand Name: Leksell Gamma Knife recall: Due to adapter not being properly aligned or locked in place
Due to adapter not being properly aligned or locked in place.
-
Class II · 7 months ago
Howmedica Osteonics Corp. MICS3 Angled Sagittal Saw Attachment recall: A potential issue was identified with the torque strength on the external
A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which…
-
Class III · 7 months ago
Datascope Corp. Battery Charging Station recall: The Battery Charging Station is an optional dual-bay charger used to charge
The Battery Charging Station is an optional dual-bay charger used to charge the Cardiosave IABP Lithium- Ion batteries when they are not being used…
-
Class II · 7 months ago
Somerset Therapeutics LLC Dexamethasone Sodium Phosphate Injection, USP, 100 mg/ 10 mL recall: Failed Impurities/Degradation Specifications - OOS impurities result observed
Failed Impurities/Degradation Specifications - OOS impurities result observed during long term stability testing at product expiry (24 months) were…
-
Class I · 7 months ago
Cardinal Health 200, LLC Webcol Alcohol Prep pad 2 ply, 200 count boxes recall: Non-Sterility: microbial contamination identified as Paenibacillus phoenicis
Non-Sterility: microbial contamination identified as Paenibacillus phoenicis
-
Class II · 7 months ago
Strides Pharma Inc Children's Ibuprofen Oral Suspension, USP, 100 mg per 5mL recall: Presence of foreign substance: the firm received complaints for a gel-like
Presence of foreign substance: the firm received complaints for a gel-like mass and black particles in the product.
-
Class II · 7 months ago
Apotex Corp. Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 0.2%/0.5%* recall: Lack of Assurance of Sterility
Lack of Assurance of Sterility
-
Public Health Alert · 7 months ago
FSIS Issues Public Health Alert for Beef and Pork Products Produced Without the Benefit of Inspection
Produced Without Benefit of Inspection
-
Class II · 7 months ago
Asukar Foods Corp TETAS Mireya, Cherry Milkshake , i unit Popsicle recall: Undeclared allergen: Soy Lecithin
Undeclared allergen: Soy Lecithin
-
Class I · 7 months ago
Bluegrass Ingredients Inc. Butter Powder, Net Weight 50 LB recall: Positive Salmonella contamination
Positive Salmonella contamination
-
Class I · 7 months ago
Bluegrass Ingredients Inc. Butter-Rich Powder, Net Weight 50 LB recall: Potential Salmonella contamination
Potential Salmonella contamination
-
Class III · 7 months ago
Winder Laboratories, LLC Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx recall: Subpotent. During an FDA inspection it was discovered that the product
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
-
Class I · 7 months ago
Amneal Magnesium Sulfate in Water for Injection, USP, 4g/100mL, IV bag recall: A Magnesium Sulfate in Water for Injection pouch was found to contain an IV
A Magnesium Sulfate in Water for Injection pouch was found to contain an IV bag of Tranexamic Acid in 0.7% Sodium Chloride Injection, 10 mg/mL.
-
NHTSA safety recall · 7 months ago
Toyota recall: The load carrying capacity modification label may display inaccurate added
The load carrying capacity modification label may display inaccurate added weight values. As such, these vehicles fail to comply with the…