Recalls affecting Rhode Island
Notices that name Rhode Island in their distribution area, plus every nationwide recall — nationwide recalls reach Rhode Island too.
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Class II · 10 months ago
Zimmer, Inc. Brand Name: Affixus Antegrade Femoral Nailing System Product Name recall: Affected implants may have undersized distal diameter along length
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk…
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Class II · 10 months ago
Zimmer, Inc. Brand Name: Affixus Antegrade Femoral Nailing System Product Name recall: Affected implants may have undersized distal diameter along length
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk…
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Class II · 10 months ago
Medtronic Neuromodulation Restore Clinician Programmer Application recall: Software issue where a Device Reset message displayed on the app was unable
Software issue where a Device Reset message displayed on the app was unable to be cleared. In rare cases, this resulted in an inability to resume…
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Class II · 10 months ago
CareFusion 303, Inc. BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer recall: Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer
Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to…
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Class II · 10 months ago
Merck Sharp & Dohme LLC Noxafil Powdermix for Delayed-Release Oral Suspension, 300 mg recall: Presence of particulate matter: potential presence of metal particulates
Presence of particulate matter: potential presence of metal particulates in the product.
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Class II · 10 months ago
Merck Emend for oral suspension, 125 mg, Single-Dose Kit recall: Presence of particulate matter: potential presence of metal particulates
Presence of particulate matter: potential presence of metal particulates in the product.
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Class I · 10 months ago
Carousel Candies Choceur Cookie Butter Holiday Bark. Standup Pouch Bag. 5 oz recall: Undeclared pecan
Undeclared pecan
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Class I · 10 months ago
Carousel Candies Choceur Pecan Cranberry & Cinnamon Holiday Bark. Standup Pouch Bag recall: Undeclared wheat
Undeclared wheat
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Class II · 10 months ago
Chips Ahoy Baked brownie bites recall: Product Safety – choking threats
Product Safety – choking threats
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Class II · 10 months ago
Gold Star Distribution All FDA-regulated products held at facility including drugs recall: Potential Salmonella contamination, presence of rodent and avian
Potential Salmonella contamination, presence of rodent and avian contamination and insanitary conditions during the storage process.
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Class II · 10 months ago
Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter recall: IFU and device kit labeling contains misleading statements leading
IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during…
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Class I · 10 months ago
GE Medical Systems China Co., Ltd. GE Healthcare Carestation anesthesia system Power recall: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia
Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power…
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Class II · 10 months ago
DICOM Grid, Inc. Intelerad InteleShare software, with ProViewer component recall: Software intended to aid in diagnosing conditions
Software intended to aid in diagnosing conditions, planning treatments, visualizing anatomical structures has a bug that, if all of following are…
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Class II · 10 months ago
Medline Industries, LP Forcep, STD STR, Sterile Kelly, 5.5 recall: The items may have weak packaging seals that may result in a breach
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if…
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Class II · 10 months ago
Medline Industries, LP Scissors, OR, Sharp/Blunt, 5.5", Sterile recall: The items may have weak packaging seals that may result in a breach
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if…
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Class II · 10 months ago
Medtronic MiniMed, Inc. InPen App, Model/CFN Number: MMT-8061 recall: When app is uninstalled and reinstalled, insulin pen software issue causes
When app is uninstalled and reinstalled, insulin pen software issue causes Choose Notification Style Screen to not show during setup so users can't…
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Class II · 10 months ago
Seaspine Orthopedics Corporation Orthofix NorthStar OCT Navigation Surgical Technique recall: The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly
The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly identified both Medtronic s Solera and Medtronic s Infinity system toolcards…
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Class II · 10 months ago
Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter recall: IFU and device kit labeling contains misleading statements leading
IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during…
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Class II · 10 months ago
Cepheid Brand Name: Xpert¿ BCR-ABL Ultra Model/ recall: Invitro diagnostic test kits with specimens that have elevated white blood
Invitro diagnostic test kits with specimens that have elevated white blood cell count (>30,000 cell) may cause inaccurate results.
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Class I · 10 months ago
GE Medical Systems China Co., Ltd. GE Healthcare Carestation anesthesia system recall: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia
Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power…
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Class II · 10 months ago
Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter recall: IFU and device kit labeling contains misleading statements leading
IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during…
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Class II · 10 months ago
Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter recall: IFU and device kit labeling contains misleading statements leading
IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during…
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Class II · 10 months ago
Brand Name: Rocket Product Name: Rocket 20Fg Seldinger Catheter recall: IFU and device kit labeling contains misleading statements leading
IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during…
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Class III · 10 months ago
Datascope Corp. Cardiosave Hybrid recall: The IFU addendum updates the Vibration and Shock Table to reference
The IFU addendum updates the Vibration and Shock Table to reference the correct standards.