Medical device recalls
38684 federal recalls on file. Federal recalls for medical devices — surgical equipment, monitors, diagnostic tools, implants, home health devices. Sourced from the FDA.
- 2024-05-08FDA-DeviceOlympus Corporation of the AmericasClass IIPOWERSEAL 5 mm, 23 cm, Curved Jaw Sealer and Divider, Double Action is indicated for use in general surgery and such surgical specialties as urologic, colorectal, bariatric, vascular, thoracic, and gynecologic. Model/Catalog Number: PS-0523CJDA
Upon initial activation of the seal function, the POWERSEAL non-conformance results in an immediate Incomplete Seal Cycle tone with the accompanying message on the generator screen, and no energy would be delivered to the device resulting in delay in surgery.
- 2024-05-08FDA-DeviceAdvanced Research Medical, LLCClass IIADVANCED RESEARCH MEDICAL Lumbar Interbody Fusion System (OLLIF), Flexible Curette Loop Blade, Part # 01-06-4; treatment of degenerative disc disease
Potential shearing of the disposable blade may occur and be contained within the of Flexible Curette Shaft Assembly during surgery.
- 2024-05-08FDA-DeviceCovidien, LPClass IISofsilk Braided Silk sutures, Product Number S-2782K. Nonabsorbable, sterile, non-mutagenic surgical suture composed of natural silk fibers, for use in soft tissue approximation and/or ligation.
One lot of product was exposed to more than the approved number of Ethylene Oxide (EO) sterilization cycles. This may decrease the tensile strength of the sutures over time, which could result in harms such as wound dehiscence, hemorrhage, blood loss, bleeding, tissue breakdown, peritonitis, unspecified infection, vision loss (when used in ophthalmic application), and/or prolonged surgery.
- 2024-05-08FDA-DeviceAdvanced Instruments, LLCClass IIOsmoPRO MAX Automated Osmometer- IVD Osmometer for Clinical Use. Uses the method of freezing point depression to measure osmolality of serum, plasma, and urine. Model/Catalog Number: OsmoPRO MAX Software Version: 1.5.0.0
System error messages may delay the ability to test patient samples and the need for frequent calibration due to results outside the expected range when testing controls.
- 2024-05-08FDA-DeviceAbbott MedicalClass IIAbbott Aveir Leadless Pacemaker, REF: LSP112V, STERILEEO
Their is a potential that electromagnetic interference may cause leadless pacemaker may result in mode change.
- 2024-05-08FDA-DeviceAllergan Sales, LLCClass IIKeller Funnel 2, REF: HA-001, STERILEEO, Rx Only,
Their is a potential that breast implants lack the lubricious coating that allows them to slide through the funnels during the implantation procedure.
- 2024-05-08FDA-DeviceThoratec Corp.Class IThoratec HeartMate 3, LVAS Implant Kit, REF:106524INT, Sterile EO, RxOnly
Potential for a leak path at the seal interface between the left ventricle assist system inflow cannula and the titanium apical cuff.
- 2024-05-08FDA-DeviceThoratec Corp.Class IThoratec HeartMate 3, LVAS Implant Kit, REF:106524US, Sterile EO, RxOnly
Potential for a leak path at the seal interface between the left ventricle assist system inflow cannula and the titanium apical cuff.
- 2024-05-08FDA-DeviceMedtronic NeuromodulationClass IIIntellis AdaptiveStim Product Number 97715, Spinal Cord Stimulator
inability to reprogram one device
- 2024-05-01FDA-DevicePhilips North America LlcClass IIPhilips Patient Information Center (PIC) iX Uninterruptable Power Supply (UPS): 1. APC (Schneider Electric IT Corporation) 120V Uninterruptable Power Supply Model: SCL500RM1U 2. APC (Schneider Electric IT Corporation) 230V Uninterruptable Power Supply Model: SCL500RMI1U
Possible failure of Uninterruptable Power Supply (UPS) devices supporting the Patient Information Center (PIC) iX system, potential for the associated PIC iX system to shut down due to the lack of power. may lead to the delay in the detection of a change in a patient condition
- 2024-05-01FDA-DeviceBaxter Healthcare CorporationClass IIBaxter Seprafilm Adhesion Barrier 1 Half Sheet, 5-PK, REF 664103, for use in abdominal and pelvic surgery
Product was distributed in the United States without proper regulatory approval.
- 2024-05-01FDA-DeviceElectro Medical Systems SAClass IIBrand Name: PIEZON Bottle Product Name: PIEZON Bottle Model/Catalog Number: EG-111 Software Version: N/A Product Description: These bottles are sold empty and are filled by the user with water - in some cases small quantities of disinfectant solutions - for dental treatments. The bottle is pressurized on the device during use. Component: YES. AIRFLOW PROPHYLAXIS MASTER and AIRFLOW PROPHYLAXIS ONE
Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or storage if the use is not releasing the pressure inside the bottles).
- 2024-05-01FDA-DeviceElectro Medical Systems SAClass IIBrand Name: WATER BOTTLE Product Name: WATER BOTTLE Model/Catalog Number: EG-121 Software Version: N/A Product Description: These bottles are sold empty and are filled by the user with water fort dental treatments. The bottle is pressurized on the device during use. Component: YES. AIRFLOW PROPHYLAXIS MASTER and AIRFLOW PROPHYLAXIS ONE
Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or storage if the use is not releasing the pressure inside the bottles).
- 2024-05-01FDA-DeviceElectro Medical Systems SAClass IIBrand Name: CLEANER BOTTLE Product Name: CLEANER BOTTLE Model/Catalog Number: EG-1000 Software Version: N/A Product Description: CLEANER bottles used with EMS AIRFLOW PROPHYLAXIS MASTER / EMS AIRFLOW ONE devices to clean the water lines. The bottle is placed on the device during cleaning. Component: YES. AIRFLOW PROPHYLAXIS MASTER and AIRFLOW PROPHYLAXIS ONE
Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or storage if the use is not releasing the pressure inside the bottles).
- 2024-05-01FDA-DeviceQuidel CorporationClass IIQUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20, 20 Tests
There are two windows on the test device, the control line window and the test results window. The line for the test results window were misaligned. In instances of positive test results, the positivite test line may not be visible/ hidden under the cassette of the test device thus potentially leading to a false negative result.
- 2024-05-01FDA-DeviceQuidel CorporationClass IIQUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20-U, 20 Tests
There are two windows on the test device, the control line window and the test results window. The line for the test results window were misaligned. In instances of positive test results, the positivite test line may not be visible/ hidden under the cassette of the test device thus potentially leading to a false negative result.
- 2024-05-01FDA-DeviceCovidien LPClass IIPalindrome Precision H Chronic Catheter Kit 14.5 Fr/Ch (4.8mm) x 23 cm (Symmetrical Tip, Heparin Coating and Tal VenaTrac Stylet- Intended for acute and chronic hemodialysis, apheresis, and infusion. Model Number (CFN): 8888145044CP
Products may not be heparin coated as indicated on the label-leads to a potential loss of benefit due to the absence of the heparin coating
- 2024-05-01FDA-DeviceCovidien LPClass IIPalindrome Precision HSI Chronic Catheter Sport Pack 14.5 Fr/Ch (4.8mm) x 19 cm (Symmetrical Tip, Heparin Coating, Silver Ion Sleeve and Tal VenaTrac Stylet- Intended for acute and chronic hemodialysis, apheresis, and infusion. Model Number (CFN): 8888119369P
Products may not be heparin coated as indicated on the label-leads to a potential loss of benefit due to the absence of the heparin coating
- 2024-05-01FDA-Device3M Company - Health Care BusinessClass II3M Durapore Surgical Tape, Catalog Number 1538-118
Select lots of the 3M Durapore Surgical Tape, Catalog Number 1538-118, were incorrectly labeled with a shelf life of 5 years, rather than 3 years.
- 2024-05-01FDA-DeviceHowmedica Osteonics Corp.Class IITRIDENTII PSL CLUSTER64H- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-64H
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
- 2024-05-01FDA-DeviceHowmedica Osteonics Corp.Class IITRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-58F
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
- 2024-05-01FDA-DeviceHowmedica Osteonics Corp.Class IITRIDENTII PSL CLUSTER52E- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-52E
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
- 2024-05-01FDA-DeviceHowmedica Osteonics Corp.Class IITRIDENTII PSL CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-50D
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
- 2024-05-01FDA-DeviceHowmedica Osteonics Corp.Class IITRIDENTII PSL CLUSTER48D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-48D
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
- 2024-05-01FDA-DeviceHowmedica Osteonics Corp.Class IITRIDENTII HEMI CLUSTER66H- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-66H
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
- 2024-05-01FDA-DeviceHowmedica Osteonics Corp.Class IITRIDENTII HEMI CLUSTER58F- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-58F
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
- 2024-05-01FDA-DeviceHowmedica Osteonics Corp.Class IITRIDENTII HEMI CLUSTER54E- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-54E
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
- 2024-05-01FDA-DeviceHowmedica Osteonics Corp.Class IITRIDENTII HEMI CLUSTER52E-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-52E
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
- 2024-05-01FDA-DeviceHowmedica Osteonics Corp.Class IITRIDENTII HEMI CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-50D
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
- 2024-05-01FDA-DeviceHowmedica Osteonics Corp.Class IITRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-48D
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
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