Latest recalls — page 303
Older notices, newest first.
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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 II · 1+ years ago
American Contract Systems, Medical Procedure kits and trays labeled recall: During an internal investigation, ACS determined that the rationale
During an internal investigation, ACS determined that the rationale for sterilization of certain components was not justified and therefore, some…
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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
Medline Kits containing BD SureStep Foley Tray Systems recall: Kits contain SureStep Foley Tray Systems recalled by BD that include
Kits contain SureStep Foley Tray Systems recalled by BD that include incorrect product information insert sheets. If a mislabeled tray is used…
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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 II · 1+ years ago
American Contract Systems, Medical Procedure kits and trays labeled recall: During an internal investigation, ACS determined that the rationale
During an internal investigation, ACS determined that the rationale for sterilization of certain components was not justified and therefore, some…
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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.