Recalls affecting Arizona
Notices that name Arizona in their distribution area, plus every nationwide recall — nationwide recalls reach Arizona too.
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Class II · 1+ years ago
GE Medical Systems, LLC GE HealthCare OEC 9800 recall: GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k)
GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in certain OEC 9800 and OEC 9900 Elite C-arm Systems. Specifically…
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Class II · 1+ years ago
Baxter Healthcare Corporation Spectrum IQ Infusion Pump, Product Code 3570009 recall: Baxter has identified that certain pumps have potentially been released
Baxter has identified that certain pumps have potentially been released with the grease applied to the cam and motor gears that will break down…
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Class III · 1+ years ago
Philips Ultrasound, Inc C5-2 Lumify Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc mC7-2 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc C8-5 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class I · 1+ years ago
Medline ReNewal Reprocessed St. Jude Medical Response and Supreme recall: Specific lots of reprocessed electrophysiology catheters may contain small
Specific lots of reprocessed electrophysiology catheters may contain small residual particulates.
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Class III · 1+ years ago
Philips Ultrasound, Inc S9-2 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class I · 1+ years ago
Tandem Diabetes Care, Inc. Battery Operated infusion pumps. t:slim X2 G5 recall: Insulin pumps manufactured with speakers from Revision A and B
Insulin pumps manufactured with speakers from Revision A and B may malfunction ("Malfunction 16") which prevents audible alerts and causes the pumps…
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Class II · 1+ years ago
Zhejiang Luyao Electronics Technology Co., Ltd. Brand Name: Homedics Product Name recall: Regulatory documentation error and misleading color packaging claim
Regulatory documentation error and misleading color packaging claim.
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Class II · 1+ years ago
GE Medical Systems, LLC GE HealthCare OEC 9900 Elite C-arm Systems recall: GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k)
GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in certain OEC 9800 and OEC 9900 Elite C-arm Systems. Specifically…
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Class III · 1+ years ago
Philips Ultrasound, Inc X7-2 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class II · 1+ years ago
The Medline General Surgery Tray is customized to meet requirements recall: Affected kits contain recalled Stryker Color Cuff Sterile Disposable
Affected kits contain recalled Stryker Color Cuff Sterile Disposable Tourniquet Cuffs. Stryker Instruments initiated this recall due to a potential…
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Class III · 1+ years ago
Philips Ultrasound, Inc L9-3 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class II · 1+ years ago
Maquet Gmbh Corin Operating Tables Model Numbers: 770001A0, 770001A2 recall: Under certain conditions, such as the simultaneous use of the operating table
Under certain conditions, such as the simultaneous use of the operating table with other medical devices, including high-frequency (HF) surgical…
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Class III · 1+ years ago
Philips Ultrasound, Inc C8-4v Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc L12-5 38mm Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc C6-2 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class II · 1+ years ago
Orascoptic Superior Visualization Dragonfly Essentials Kit recall: Due to complaints, loupe nose pads containing nickel may cause an allergic
Due to complaints, loupe nose pads containing nickel may cause an allergic reaction.
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Class III · 1+ years ago
Philips Ultrasound, Inc Transducer L12-5 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class II · 1+ years ago
MEDLINE INDUSTRIES, LP - Northfield H-E-B, inControl, Sterile* Alcohol Pads recall: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration
Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
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Class II · 1+ years ago
MEDLINE INDUSTRIES, LP - Northfield Rite AID Pharmacy, first aid alcohol prep pads recall: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration
Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
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Class II · 1+ years ago
Amerisource Health Services LLC Sucralfate Tablets, USP 1 gram, 100 Tablets recall: CGMP Deviations: The recalling firm filed for Chapter 11 in September 2024
CGMP Deviations: The recalling firm filed for Chapter 11 in September 2024. As a result, it cannot monitor the quality program and hence cannot…
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Class II · 1+ years ago
Lannett Company Inc. Lisdexamfetamine Dimesylate Capsules, 40 mg, 100-count bottles recall: Labeling: Label Mix-up. A bottle labeled as Lisdexamphetamine Dimesylate
Labeling: Label Mix-up. A bottle labeled as Lisdexamphetamine Dimesylate Capsules 40mg, contained Lisdexamphetamine Dimesylate Capsules 30mg.
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Class II · 1+ years ago
Medline Alcohol Prep Pads, 70% Isopropyl Alcohol recall: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration
Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.