Recalls affecting Pennsylvania
Notices that name Pennsylvania in their distribution area, plus every nationwide recall — nationwide recalls reach Pennsylvania too.
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Highest risk · 3 months ago
Golden Link Fantastic Four Cups and Captain America Popcorn Helmet Containers recall: Risk of Serious Injury or Death from Battery Ingestion Hazard
Risk of Serious Injury or Death from Battery Ingestion Hazard; Violate Mandatory Standard for Consumer Products with Button Cell Batteries
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Highest risk · 3 months ago
Galanz Americas Retro Refrigerators recall: Risk of Serious Injury or Death from Fire and Burn Hazards; One Death Reported
Risk of Serious Injury or Death from Fire and Burn Hazards; One Death Reported
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Class II · 3 months ago
Olympus 4K UHD LCD Monitor recall: Potential for the HDMI and DisplayPort (DP) connectors can become faulty
Potential for the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities.
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Class II · 3 months ago
Boston Scientific Corporation Faradrive Steerable Sheath - US recall: Boston Scientific's complaint investigations have identified that a subset
Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage…
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Class II · 3 months ago
Boston Scientific Corporation Faradrive Steerable Sheath Clear IDE recall: Boston Scientific's complaint investigations have identified that a subset
Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage…
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Class II · 3 months ago
Prismatik Dentalcraft, Inc. Brand Name: Silent Nite Product Name: Silent Nite Sleep recall: Due to device not having FDA Clearance
Due to device not having FDA Clearance
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Class II · 3 months ago
PIE Medical Imaging B.V. 3mensio Workstation software recall: User measurement value reported by diagnostic bioimaging software intended
User measurement value reported by diagnostic bioimaging software intended to measure/visualize cardiovascular structures may be larger (0.8% to…
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Class II · 3 months ago
SeaSpine Polyaxial Head REF Number: 41-3010 recall: Due to manufacturing error, polyaxial head may popoff from the screw
Due to manufacturing error, polyaxial head may popoff from the screw intraoperatively following insertion.
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Class II · 3 months ago
Boston Scientific Corporation Faradrive Steerable Sheath Clear OUS recall: Boston Scientific's complaint investigations have identified that a subset
Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage…
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Class II · 3 months ago
Emano Flow with software version v2.0.0 GS1 GTIN code: 199874903484 recall: Problem description/Reason for recall: During the period March 22, 2026
Problem description/Reason for recall: During the period March 22, 2026, to May 29, 2026, recorded urination audio was captured at 48,000 Hz while…
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Class II · 3 months ago
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters 5cc recall: Affected kits contain recalled Bard Silastic Foley Catheters. Catheters
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present…
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Class II · 3 months ago
Boston Scientific TheraSphere 360 Y-90 Management Platform recall: Software anomaly occurs when a user adds one or more vials to the cart
Software anomaly occurs when a user adds one or more vials to the cart and subsequently returns to the Activity Calculator to modify one or more…
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Class II · 3 months ago
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters 5cc recall: Affected kits contain recalled Bard Silastic Foley Catheters. Catheters
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present…
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Class II · 3 months ago
Olympus High Flow Insufflation Unit - UHI-4 recall: Potential for unexpected instances where the front panel display turns off
Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases.
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Class II · 3 months ago
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters 5cc recall: Affected kits contain recalled Bard Silastic Foley Catheters. Catheters
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present…
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Class II · 3 months ago
Micro Therapeutics, Inc. Pipeline Flex Embolization Device with Shield Technology recall: Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants
Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants…
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Class II · 3 months ago
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters 5cc recall: Affected kits contain recalled Bard Silastic Foley Catheters. Catheters
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present…
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Class II · 3 months ago
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters 5cc recall: Affected kits contain recalled Bard Silastic Foley Catheters. Catheters
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present…
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Class II · 3 months ago
Kent Imaging, Inc. SnapshotGLO Wound Imaging Device, Model KB100, KB100AA recall: The software controlling the wound imaging device's battery charging circuit
The software controlling the wound imaging device's battery charging circuit was not designed to recognize and recover a battery that has fully…
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Class II · 3 months ago
AVID Medical, Inc. Halyard EYE PACK. Model/ recall: Incorrect concentration of Betadine solution contained within certain AVID
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
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Class II · 3 months ago
Wilcox Industries Corp recall: Wilcox is notifying all customers who have purchased a product from the BOSS
Wilcox is notifying all customers who have purchased a product from the BOSS Xe family that a software enhancement to increase safety has been…
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Class II · 3 months ago
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters 5cc recall: Affected kits contain recalled Bard Silastic Foley Catheters. Catheters
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present…
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Class II · 3 months ago
Paragon 28, Inc. P28 Phanton Intramedullary Nail System, Phantom Hindfoot TTC/TC Ball recall: Paragon 28 received two (2) complaints were received involving breaches
Paragon 28 received two (2) complaints were received involving breaches in the sterile barrier of the pouch packaging.
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Class II · 3 months ago
Micro Therapeutics, Inc. Pipeline Flex Embolization Device with Shield Technology recall: Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants
Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants…