Medical DeviceSep 4, 2024
Schiller, Ag CARDIOVIT AT-180 recall — FDA Z-2734-2024
Potential for high-frequency signal artifacts is recorded during an ECG acquisition performed by CARDIOVIT AT-180 electrocardiographs.
Class IIFDA: OngoingSchiller, Ag
Monthly breakdown
2024 recalls by month
Select a month to review the recall records reported during that period.
December 2024325 records · 4 categoriesNovember 2024355 records · 4 categoriesOctober 2024409 records · 4 categoriesSeptember 2024547 records · 4 categoriesAugust 2024327 records · 4 categoriesJuly 2024318 records · 4 categoriesJune 2024286 records · 4 categoriesMay 2024422 records · 4 categoriesApril 2024323 records · 4 categoriesMarch 2024332 records · 4 categoriesFebruary 2024425 records · 4 categoriesJanuary 2024298 records · 4 categories
2024 recalls — page 60
Records are ordered by the best available source date.
Medical DeviceSep 4, 2024
Beaver Visitec International BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and recall — FDA Z-2797-2024
Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in…
Class IIFDA: OngoingBeaver Visitec International, Inc.
Medical DeviceSep 4, 2024
Medline procedural kits labeled as: 1) PERIPHERAL ULTRASOUND CATHETER INSERTION, Pack Number recall — FDA Z-2742-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 4, 2024
Medline procedural kits labeled as: 1) BOTOX KIT - CHRONIC MIGRAINE, Pack Number DYKM2000 recall — FDA Z-2750-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 4, 2024
Beaver Visitec International BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and recall — FDA Z-2790-2024
Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in…
Class IIFDA: OngoingBeaver Visitec International, Inc.
Medical DeviceSep 4, 2024
Beaver Visitec International BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and recall — FDA Z-2915-2024
Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in…
Class IIFDA: OngoingBeaver Visitec International, Inc.
Medical DeviceSep 4, 2024
MEDLINE INDUSTRIES, LP - Northfield Centurion procedure packs, containing Caina syringes recall — FDA Z-2778-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 4, 2024
Beaver Visitec International BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and recall — FDA Z-2827-2024
Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in…
Class IIFDA: OngoingBeaver Visitec International, Inc.
Medical DeviceSep 4, 2024
Medline procedural kits labeled as: 1) FETAL SURGERY-LF, Pack Number CDS840214Q recall — FDA Z-2748-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 4, 2024
Beaver Visitec International BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and recall — FDA Z-2885-2024
Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in…
Class IIFDA: OngoingBeaver Visitec International, Inc.
Medical DeviceSep 4, 2024
Beaver Visitec International BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and recall — FDA Z-2786-2024
Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in…
Class IIFDA: OngoingBeaver Visitec International, Inc.
Medical DeviceSep 4, 2024
ORTHOPEDIATRICS CANADA ULC Dba PEGA MEDICAL FRT250 - 4.0-6.4 CARTRIDGE recall — FDA Z-2941-2024
During the assembly of the FRT250 cartridge assembly, an incorrect component was used. Specifically, the FRT240-HEX (2) was used instead of the FRT250-HEX.
Class IIFDA: OngoingORTHOPEDIATRICS CANADA ULC Dba PEGA MEDICAL
Medical DeviceSep 4, 2024
Beaver Visitec International BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and recall — FDA Z-2925-2024
Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in…
Class IIFDA: OngoingBeaver Visitec International, Inc.
Medical DeviceSep 4, 2024
Medline procedural kits labeled as: 1) BIOPSY PACK, Pack Number DYNJ63370A recall — FDA Z-2746-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 4, 2024
Beaver Visitec International BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and recall — FDA Z-2865-2024
Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in…
Class IIFDA: OngoingBeaver Visitec International, Inc.
Medical DeviceSep 4, 2024
Medline procedure packs containing Shenli syringes, labeled as follows: 1) CVC DOUBLE LUMEN recall — FDA Z-2631-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 4, 2024
Beaver Visitec International BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and recall — FDA Z-2889-2024
Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in…
Class IIFDA: OngoingBeaver Visitec International, Inc.
Medical DeviceSep 4, 2024
Smiths Medical ASD PORTEX Bivona Tracheostomy Silicone Tube, labeled as: TTS NEONATAL TRACHY recall — FDA Z-2607-2024
Smiths Medical has identified that the securement flange of specific lots of the Bivona Neonatal/Pediatric and Adult Tracheostomy products may tear because of a manufacturing defect.
Class IFDA: OngoingSmiths Medical ASD Inc.
Medical DeviceSep 4, 2024
Beaver Visitec International BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and recall — FDA Z-2936-2024
Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in…
Class IIFDA: OngoingBeaver Visitec International, Inc.
Medical DeviceSep 4, 2024
Beaver Visitec International BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and recall — FDA Z-2884-2024
Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in…
Class IIFDA: OngoingBeaver Visitec International, Inc.
Medical DeviceSep 4, 2024
Beaver Visitec International BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and recall — FDA Z-2930-2024
Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in…
Class IIFDA: OngoingBeaver Visitec International, Inc.
Medical DeviceSep 4, 2024
Beaver Visitec International BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and recall — FDA Z-2849-2024
Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in…
Class IIFDA: OngoingBeaver Visitec International, Inc.
Medical DeviceSep 4, 2024
MEDLINE INDUSTRIES, LP - Northfield See RES description recall — FDA Z-2628-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 4, 2024
Beaver Visitec International BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and recall — FDA Z-2837-2024
Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in…
Class IIFDA: OngoingBeaver Visitec International, Inc.
About the 2024 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.