Recalls affecting Illinois
Notices that name Illinois in their distribution area, plus every nationwide recall — nationwide recalls reach Illinois too.
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Class II · last month
American Contract System Convenience Kit, D & C PACK, Model/ recall: The Convenience Kits contain Medline's Red Rubber Intermittent Catheters
The Convenience Kits contain Medline's Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries…
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Class II · last month
AVID Medical, Inc. Halyard Total Joint Model/ recall: Labeling Deficiency: The medical kit labeling fails to identify
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
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Class II · last month
AVID Medical, Inc. Brand Name: Halyard Product Name: Davinci Trucustom Bundle recall: Labeling Deficiency: The medical kit labeling fails to identify
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
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Class II · last month
Medline convenience kits labeled as: LTP CDS-LF recall: Kits contain a potentially contaminated component which were recalled
Kits contain a potentially contaminated component which were recalled by the manufacturer
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Class II · last month
AVID Medical, Inc. Halyard Total Joint Model/ recall: Labeling Deficiency: The medical kit labeling fails to identify
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
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Class II · last month
Medline Hudson RCI, Dbd-Circuit,Vent,Inspiratory,Heated,NEO recall: Neonatal and infant heated wire breathing circuits may experience sporadic
Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit…
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Class II · last month
Medline medical convenience kits, labeled as: 1) Sinus Pack-Lf recall: Specific item(s) and lot(s) of Medline convenience kits containing Pilling
Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to…
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Class II · last month
Canon Medical System, USA, INC. Alphenix Models Infx-8000C Infx-8000F Infx-8000V recall: Due to the fixing screws of ceiling movement gear in ceiling suspended arm
Due to the fixing screws of ceiling movement gear in ceiling suspended arm that are part of the X-ray interventional systems may become loose.
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Class II · last month
Merge Pacs and Merge OrthoPacs, medical imaging diagnostic workstation recall: Software issue may cause measurements to be displayed inaccurately
Software issue may cause measurements to be displayed inaccurately.
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Class II · last month
Fresenius Medical Care, 2008T BlueStar Hemodialysis Machine recall: Fresenius Medical Care Renal Therapies Group
Fresenius Medical Care Renal Therapies Group, LLC (FMCRTG) has received complaints regarding flow-, no water-, or temperature-related alarms with the…
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Class II · last month
Olympus Corporation of the Americas Powerseal 5 MM 23 CM , Curved Jaw Sealer & Divider recall: Potential labeling deficiency in which an outer shelf box is incorrectly
Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device.
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Class II · last month
Medline convenience kits labeled as: 1) C-Section recall: Kits contain a potentially contaminated component which were recalled
Kits contain a potentially contaminated component which were recalled by the manufacturer
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Class II · last month
IMRIS Imaging Inc ORT300, operating room table, ORT300 Modular Table Main Unit Assy recall: The linear actuator and rotational lock mechanism components may experience
The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between…
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Class II · last month
Medline breathing circuits labeled as: 1) Hudson RCI, Circuit, HTD recall: Neonatal and infant heated wire breathing circuits may experience sporadic
Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit…
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Class II · last month
IMRIS Imaging Inc ORT200, operating room table, including the ORT200 Covered Table recall: The linear actuator and rotational lock mechanism components may experience
The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between…
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Class II · last month
Medline convenience kits labeled as: 1) Major Procedure recall: Kits contain a potentially contaminated component which were recalled
Kits contain a potentially contaminated component which were recalled by the manufacturer
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Class II · last month
Medline convenience kits labeled as: 1) CMH Litho Minor Pack-Lf recall: Kits contain a potentially contaminated component which were recalled
Kits contain a potentially contaminated component which were recalled by the manufacturer
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Class II · last month
Medline convenience kits labeled as: 1) Lami Fusion recall: Kits contain a potentially contaminated component which were recalled
Kits contain a potentially contaminated component which were recalled by the manufacturer
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Class II · last month
Apotex Corp. Paxil CR, Paroxetine, Extended-Release Tablets, 37.5mg, 30 count bottle recall: Failed Dissolution Specifications; product failed to meet 24-month stability
Failed Dissolution Specifications; product failed to meet 24-month stability testing acceptance criteria
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Class II · last month
Accord Healthcare, Inc. Levothyroxine Sodium Tablets, USP, 112 mcg recall: Subpotent Drug
Subpotent Drug
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Class II · last month
Accord Healthcare, Inc. Levothyroxine Sodium Tablets, USP, 88 mcg , 1000-count bottles recall: Subpotent Drug
Subpotent Drug
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Class II · last month
Accord Healthcare, Inc. Levothyroxine Sodium Tablets, USP, 100 mcg recall: Subpotent Drug
Subpotent Drug
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Class I · last month
B Braun Medical Inc Lactated Ringer's Injection USP, 1000 mL EXCEL container recall: Presence of Particulate matter
Presence of Particulate matter.
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Class I · last month
Fresenius Kabi USA, LLC Tyenne Injection, 400 mg/20 mL , 20 mL vial recall: Presence of particulate matter:An internal investigation at the firm found
Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles.