Recalls affecting Puerto Rico
Notices that name Puerto Rico in their distribution area, plus every nationwide recall — nationwide recalls reach Puerto Rico too.
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Class II · 2 months ago
Shilpa Medicare Limited Pemrydi RTU , 100 mg/10 mL , Single-dose vial recall: Discolored solution. The firm has received market complaints reporting green
Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials
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Class II · 2 months ago
American Regent, Inc. Acetylcysteine Solution, USP, 10% , packaged in a) 4 mL Vial recall: Presence of Particulate Matter: Product contaminated with particulate matter
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
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Class I · 2 months ago
American Regent, Inc. Papaverine HCl Injection, USP, 60 mg/2 mL recall: Presence of Particulate Matter: Product contaminated with particulate matter
Presence of Particulate Matter: Product contaminated with particulate matter identified as glass and/or paraformaldehyde
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Class II · 2 months ago
American Regent, Inc. Acetylcysteine Solution, USP, 20% , packaged in a) 4 mL Vial recall: Presence of Particulate Matter: Product contaminated with particulate matter
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
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Class II · 2 months ago
American Regent, Inc. Multrys , For intravenous infusion recall: Presence of Particulate Matter: Product contaminated with particulate matter
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
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Class II · 2 months ago
Golden State Medical Supply Inc. Carbamazepine Tablets, USP, 200mg recall: CGMP deviations: tablets with black specks
CGMP deviations: tablets with black specks.
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Class II · 2 months ago
American Regent, Inc. Cyanocobalamin injection USP, 10,000 mcg/10 mL recall: Presence of Particulate Matter: Product contaminated with particulate matter
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
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Class I · 2 months ago
Jalapeno Pepper packaged in bulk generic Coast Tropical cardboard recall: Potential Salmonella Javiana contamination
Potential Salmonella Javiana contamination
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NHTSA safety recall · 2 months ago
Mitsubishi Outlander and Outlander PHEV recall: Due to improper software programming, the Alliance In-Vehicle Infotainment
Due to improper software programming, the Alliance In-Vehicle Infotainment (A-IVI) system may fail to display the rearview camera image when the…
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NHTSA safety recall · 2 months ago
Ford Mustang recall: The engine compartment wiring harness ground connections may fracture
The engine compartment wiring harness ground connections may fracture and result in a loss of drive power, or a loss of function in the windshield…
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NHTSA safety recall · 2 months ago
Kia EV9 recall: Due to improper routing, the Occupant Detection System (ODS)
Due to improper routing, the Occupant Detection System (ODS) may not deactivate the air bag when a child or child seat is in the front passenger…
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NHTSA safety recall · 2 months ago
Marathon Industries recall: The deck pins may break, resulting in the liftgate platform falling
The deck pins may break, resulting in the liftgate platform falling.
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NHTSA safety recall · 2 months ago
General recall: The rearview camera screen may display a distorted or blank image
The rearview camera screen may display a distorted or blank image.
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Highest risk · 2 months ago
Modine Manufacturing Company Airedale Heating and Cooling Ventilation Fans recall: Fire Hazard
Fire Hazard
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Highest risk · 2 months ago
KTM North America Off-Road Motorcycles recall: Risk of Serious Injury or Death from Crash Hazard
Risk of Serious Injury or Death from Crash Hazard
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Highest risk · 2 months ago
Goal Zero YETI 3000X Power Stations recall: Serious Risk of Injury from Fire and Burn Hazards
Serious Risk of Injury from Fire and Burn Hazards
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Class II · 2 months ago
Biofire Respiratory Panel 2.1 REF 423742 UDI code: 00815381020529 recall: Due to increase in false negative results
Due to increase in false negative results
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Class II · 2 months ago
OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light recall: There is a potential for vaginal speculums to contain a burr on the proximal
There is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions…
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Class II · 2 months ago
Covidien, LP Dermalon 88861757-31 Dermalon* 4-0 BLU 75CM C13 88861757-31 88861799-31 recall: Product may contain a perforation or tear in the sterile barrier packaging
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which…
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Class II · 2 months ago
Cardinal Health Presource Kits: 1) Basic Pack recall: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
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Class II · 2 months ago
Covidien, LP Surgipro SP-623 Surgipro* 2-0 BLU 75CM SC2 X36 SP-623 recall: Product may contain a perforation or tear in the sterile barrier packaging
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which…
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Class II · 2 months ago
Straumann USA LLC GM Helix Implant, Endosseous Dental Implant Article No. 109.984 recall: There may be a mismatch between the implant contained inside the packaging
There may be a mismatch between the implant contained inside the packaging and the information described on the outer carton label. If the the…
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Class II · 2 months ago
Cardinal Health Presource Kits: 1) Septo Rhino Pack recall: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
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Class II · 2 months ago
Spacelabs Healthcare, Inc. Brand Name: Xhibit Product Name: Xhibit Central Station recall: Due to off-the-shelf display port component that has audio/video failures
Due to off-the-shelf display port component that has audio/video failures