Recalls affecting Maryland
Notices that name Maryland in their distribution area, plus every nationwide recall — nationwide recalls reach Maryland too.
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Class II · last month
Maquet Cardiopulmonary Gmbh Percutaneous Insertion Kit , Guidewire 150 cm recall: The packaging may not consistently maintain sterile barrier integrity
The packaging may not consistently maintain sterile barrier integrity.
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Class I · last month
Abiomed, Inc. Impella Optical Controller, Automated Impella Controller recall: The potential for purge cassette recognition issues due to the failure
The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly.
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Class II · last month
Boston Scientific Corporation StoneSmart Connect Console Contents recall: A subset of power adapters used with the connect console may exhibit
A subset of power adapters used with the connect console may exhibit higher-than-expected resistance in the electrical grounding path. As a result…
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Class I · last month
Medline Convenience Kits: 1) DYNDB3086D recall: The kits contain certain lots of sterile applicators which may contain fungal
The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions…
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Class I · last month
Medline Convenience Kits: 1) Open Heart Adult recall: The kits contain certain lots of sterile applicators which may contain fungal
The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions…
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Class II · last month
GE Healthcare Centricity Enterprise Archive V2, V3, and V4 recall: Under certain conditions historical imaging data migrated from a legacy
Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this…
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Class II · last month
ICU Medical, Inc. IV Non-Dedicated Gravity Administration Sets with drip chambers recall: Intravascular administration tubing set drip chambers may have black specks
Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored…
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Class II · last month
Howmedica Osteonics Corp. Trident 0¿ Poly Insert 28mm ID 620-00-28D Orthopaedic recall: Affected devices were manufactured with Ultra High Molecular Weight
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the…
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Class II · last month
Howmedica Osteonics Corp. Omnifit Series I Acet. Insert 10¿ 22mm ID recall: Affected devices were manufactured with Ultra High Molecular Weight
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the…
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Class I · last month
Medline Convenience Kits: 1) DYNDH1193 recall: The kits contain certain lots of sterile applicators which may contain fungal
The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions…
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Class I · last month
Abiomed, Inc. Impella Optical Controller with the below product descriptions recall: The potential for purge cassette recognition issues due to the failure
The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly.
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Class II · last month
Maquet Cardiopulmonary Gmbh Percutaneous Insertion Kit , Guidewire 100 cm recall: The packaging may not consistently maintain sterile barrier integrity
The packaging may not consistently maintain sterile barrier integrity.
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Class II · last month
Wilson-Cook Medical Inc. Brand Name: Hemospray Endoscopic Hemostat Product Name recall: Due to issue with endoscope adherence and inability to spray powder. Firm
Due to issue with endoscope adherence and inability to spray powder. Firm will provide an updated Instruction for Use (IFU).
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Class II · last month
Bayer Medical Care, Inc. Medrad¿ Stellant Flex Syringe Kit used with Stellant Flex CT recall: Some devices may not have been properly sterilized due to a manufacturing
Some devices may not have been properly sterilized due to a manufacturing sterilization issue.
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Class II · last month
Pi Cardia Ltd Pi-Cardia Inc. ShortCut REF: Z-A-20.003-US recall: Transfemoral catheter, positing arm may detached due to weld issue
Transfemoral catheter, positing arm may detached due to weld issue.
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Class II · last month
GE Healthcare Centricity PACS V2, V3, V4, V6, V7, software product is intended recall: Under certain conditions historical imaging data migrated from a legacy
Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this…
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Class II · last month
Stryker Sustainability Solutions REF:B5LT Ethicon Endo-Surgery recall: Reusable access port system may crack or seperate during use
Reusable access port system may crack or seperate during use.
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Class II · last month
Howmedica Osteonics Corp. Acetabular CUP Uhmwpe 61-3258 ALL Poly Constrained Insert recall: Affected devices were manufactured with Ultra High Molecular Weight
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the…
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Class II · last month
Howmedica Osteonics Corp. ABG I Acetabular Insert Hooded 28mm ID X 48mm C-M079-2-801 recall: Affected devices were manufactured with Ultra High Molecular Weight
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the…
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Class II · last month
Mirion Technologies , Inc. Captus 4000e Thyroid Uptake System, Models: 1. 5430-30151 recall: Potential for failure of the tension bolt which would allow the spring arm
Potential for failure of the tension bolt which would allow the spring arm to unexpectedly fall to its lowest position, which is approximately 25…
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Class II · last month
Stryker Sustainability Solutions REF:B5ST Ethicon Endo-Surgery recall: Reusable access port system may crack or seperate during use
Reusable access port system may crack or seperate during use.
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Class II · last month
F & A Foundation Reign Medical Clench Staple System , Description/REF: 9mm x recall: Bone fixation staple requires a new 510(k); the performance characteristics
Bone fixation staple requires a new 510(k); the performance characteristics of this device have not been adequately established.
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Class II · last month
Howmedica Osteonics Corp. Scorpio C-Dome Patella 73-2710 73-2910 Scorpio U-Dome recall: Affected devices were manufactured with Ultra High Molecular Weight
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the…
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Class I · last month
Medline Convenience Kits: 1) KIT Anesthesia L&D A- Line SET recall: The kits contain certain lots of sterile applicators which may contain fungal
The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions…