Recalls affecting Kansas
Notices that name Kansas in their distribution area, plus every nationwide recall — nationwide recalls reach Kansas too.
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Class II · 1+ years ago
Philips North America Cardiac Workstation 5000 recall: Failure of Environmental Stress Testing from a pinched power module wire
Failure of Environmental Stress Testing from a pinched power module wire within the housing of the Cardiac Workstation device which resulted in a…
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Class I · 1+ years ago
Bronchovideoscope Olympus BF-1TH1100 recall: Additional IFU updates to provide further clarification on safe and effective
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma…
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Class II · 1+ years ago
Baxter Healthcare Corporation Clearlink System Extension SET recall: IV sets may leak
IV sets may leak.
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Class II · 1+ years ago
American Contract Systems Inc. Medical convenience kits recall: Identified products were re-gassed (sterilized more than once) after
Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection…
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Class II · 1+ years ago
American Contract Systems Inc. Medical convenience kits recall: Identified products were re-gassed (sterilized more than once) after
Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection…
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Class I · 1+ years ago
Evis Exera II Bronchovideoscope Olympus BF Type 1T180 recall: Additional IFU updates to provide further clarification on safe and effective
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma…
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Class I · 1+ years ago
Bronchovideoscope Olympus BF Type P150 recall: Additional IFU updates to provide further clarification on safe and effective
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma…
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Class II · 1+ years ago
Boston Scientific Corporation Tenacio Pump without InhibiZone recall: The potential for devices to experience inflation and/or deflation
The potential for devices to experience inflation and/or deflation performance issues or difficulties.
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Class II · 1+ years ago
Ferno-Washington Inc Ferno Power X2 Powered Ambulance COT, Model/ recall: The fastening post hardware could loosen allowing the fastening post
The fastening post hardware could loosen allowing the fastening post to detach from the cot
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Class II · 1+ years ago
Baxter Healthcare Corporation Clearlink System Continu-Flo Solution Set, Non-Vented recall: IV sets may leak
IV sets may leak.
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Class I · 1+ years ago
OES Bronchofiberscope Olympus BF Type 1T60 recall: Additional IFU updates to provide further clarification on safe and effective
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma…
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Class I · 1+ years ago
Bronchofiberscope Olympus BF Type TE2 recall: Additional IFU updates to provide further clarification on safe and effective
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma…
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Class I · 1+ years ago
OES Bronchofiberscope Olympus BF Type XT40 recall: Additional IFU updates to provide further clarification on safe and effective
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma…
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Class II · 1+ years ago
GE Medical Systems, LLC LOGIQ P10 R4.5 HD ultrasound system with system software recall: The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data
The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could…
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Class II · 1+ years ago
American Contract Systems Inc. Medical convenience kits recall: Identified products were re-gassed (sterilized more than once) after
Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection…
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Class II · 1+ years ago
Baxter Healthcare Corporation Clearlink System Continu-Flo Solution Set, Non-Vented recall: IV sets may leak
IV sets may leak.
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Class I · 1+ years ago
Evis Exera Bronchovideoscope Olympus BF Type XT160 recall: Additional IFU updates to provide further clarification on safe and effective
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma…
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Class II · 1+ years ago
Baxter Healthcare Corporation Clearlink System Solution Set, Duo-Vent recall: IV sets may leak
IV sets may leak.
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Class II · 1+ years ago
SV Labs Prescott Corporation Aloe Up Sport Performance Sunscreen Lotion SPF 30 recall: cGMP deviations: the firm released and distributed product which failed total
cGMP deviations: the firm released and distributed product which failed total aerobic microbial count testing.
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Class III · 1+ years ago
Endo USA, Inc. Everolimus tablets 5mg, 28 tablets recall: Failed Impurities/Degradation Specifications: Out of specification
Failed Impurities/Degradation Specifications: Out of specification for impurity IP-C.
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Class II · 1+ years ago
Glenmark Pharmaceuticals Inc., USA Viorele, Desogestrel and Ethinyl Estradiol, USP recall: Failed Impurities/Degradation Specifications
Failed Impurities/Degradation Specifications
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Class III · 1+ years ago
STAQ Pharma, Inc. FentaNYL Citrate PF, 500mcg/50 mL in Nacl, Injection for IV use recall: Labeling: Incorrect or Missing Lot and/or Exp Date
Labeling: Incorrect or Missing Lot and/or Exp Date
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Class III · 1+ years ago
STAQ Pharma, Inc. Hydromorphone HCL PF, 10mg/50 mL in Nacl, Injection for IV use recall: Labeling: Incorrect or Missing Lot and/or Exp Date
Labeling: Incorrect or Missing Lot and/or Exp Date
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Class II · 1+ years ago
Ascend Laboratories, LLC Atorvastatin Calcium Tablets USP, 40 mg recall: Failed Dissolution Specifications
Failed Dissolution Specifications