Medical DeviceFeb 19, 2020
Microvention Terumo AZUR Peripheral Coil System, Detachable 18, Framing Coil, REF numbers recall — FDA Z-1221-2020
The devices may be missing the implant coil.
Class IIFDA: TerminatedMicrovention, Inc.
Latest records
Latest recalls — page 1079
The newest recall records with useful source details are listed here.
Medical DeviceFeb 19, 2020
Arrow International 10 cc Luer-Slip Loss of Resistance Syringe, Product Code LR-05501 recall — FDA Z-1205-2020
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceFeb 19, 2020
Pacific Medical Group Toco MP Transducer (M2734B), that may have been serviced with the recall — FDA Z-1168-2020
Fetal/maternal monitor/monitoring systems serviced or remanufactured using non-OEM equivalent components that have not been appropriately verified or validated. Possible adverse clinical…
Class IIFDA: OngoingPacific Medical Group Inc.
Medical DeviceFeb 19, 2020
Arrow International EPIDURAL CATHETERIZATION KIT, Product Code UR-05501-EXP recall — FDA Z-1215-2020
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceFeb 19, 2020
Arrow International FlexTip Plus Epidural Catheterization Set, Product Code MP-17019-TIP recall — FDA Z-1206-2020
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceFeb 19, 2020
Pacific Medical Group Loop-Style Tocotransducer (Nautilus) 2264LAX, that may have been recall — FDA Z-1160-2020
Fetal/maternal monitor/monitoring systems serviced or remanufactured using non-OEM equivalent components that have not been appropriately verified or validated. Possible adverse clinical…
Class IIFDA: OngoingPacific Medical Group Inc.
Medical DeviceFeb 19, 2020
Arrow International EPIDURAL CATHETERIZATION KIT, Product Code DE-05400D-BO recall — FDA Z-1195-2020
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceFeb 19, 2020
Arrow International TheraCath Epidural Catheterization Kit, Product Code ASK-05001-SLR1 recall — FDA Z-1175-2020
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceFeb 19, 2020
Arrow International FlexTip Plus Epidural Catheterization Set, Product Code AA-05400-E recall — FDA Z-1171-2020
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceFeb 19, 2020
C.R. Bard The Bard Intra-abdominal Pressure Monitoring Device is composed of a tubing set recall — FDA Z-1219-2020
Leaks or disconnect near the sampling port of the Intra Abdominal Pressure Monitoring Device which could lead to the potential of inaccurate readings. The measurement should be confirmed…
Class IIFDA: TerminatedC.R. Bard Inc.
Medical DeviceFeb 19, 2020
Pacific Medical Group Ultrasound Transducer (M1356A), that may have been serviced with the recall — FDA Z-1164-2020
Fetal/maternal monitor/monitoring systems serviced or remanufactured using non-OEM equivalent components that have not been appropriately verified or validated. Possible adverse clinical…
Class IIFDA: OngoingPacific Medical Group Inc.
Medical DeviceFeb 19, 2020
TELEFLEX MEDICAL HUDSON RCI COMFORT FLO Humidification System, REF 2410, humidifier recall — FDA Z-1114-2020
There is the potential for water to flood the column and enter the circuit under circumstances where an abnormal pressure differential is created between the water bottle and the column…
Class IFDA: TerminatedTELEFLEX MEDICAL Inc.
Medical DeviceFeb 19, 2020
DePuy Orthopaedics SPECIALIST 2 DISTAL FEMORAL CUTTING BLOCK recall — FDA Z-1169-2020
The device will not connect to the Specialist 2 Locating Outrigger which renders them unusable in surgery.
Class IIFDA: TerminatedDePuy Orthopaedics, Inc.
Medical DeviceFeb 19, 2020
Arrow International FlexTip Plus Epidural Catheterization Set for Pediatric Lumbar recall — FDA Z-1196-2020
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceFeb 19, 2020
Arrow International FlexTip Plus Epidural Catheterization Set, Product Code JC-05400-DCS recall — FDA Z-1202-2020
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceFeb 19, 2020
Arrow International EPIDURAL CATHETERIZATION KIT, Product Code JC-05400-LB recall — FDA Z-1204-2020
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceFeb 19, 2020
TELEFLEX MEDICAL Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System recall — FDA Z-1117-2020
The products are being recalled due to reports of breakage broke at the point of a welded joint either prior to use during setup or during use inside the patient's mouth.
Class IIFDA: TerminatedTELEFLEX MEDICAL Inc.
Medical DeviceFeb 19, 2020
Arrow International EPIDURAL CATHETERIZATION KIT, Product Code IT-05400-DC recall — FDA Z-1200-2020
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceFeb 19, 2020
Arrow International FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05400-CA1 recall — FDA Z-1179-2020
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceFeb 19, 2020
Tytek Medical PneumoDart, 14 ga x 3.25in., REF TM-317 A compact, sterile, device intended recall — FDA Z-0930-2020
A defect involving an occluded needle was discovered during a training exercise.
Class IFDA: TerminatedTytek Medical Inc.
Medical DeviceFeb 19, 2020
Arrow International Epidural Catheterization Kit with FlexTip Plus, Open Tip, Single- Port recall — FDA Z-1181-2020
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceFeb 19, 2020
Microvention Terumo AZUR CX Peripheral Coil System, Detachable 35, CX Coil, REF numbers recall — FDA Z-1225-2020
The devices may be missing the implant coil.
Class IIFDA: TerminatedMicrovention, Inc.
FoodFeb 19, 2020
Market bliss anti-stress formula Dietary Supplement, 60 Tablets recall — FDA F-0681-2020
Potentially undeclared Yohimbe 83 and complaints of adverse reactions: upset stomach, jittery, sweaty, lightheaded or dizzy.
Class IIFDA: CompletedMarket America Inc.
FoodFeb 19, 2020
Sugar Foods DISTRIBUTED BY FOODHOLD USA, LLC, LANDOVER, MD 20758 UPC 6 recall — FDA F-0736-2020
They were notified by their supplier that the product may be contaminated with foreign material.
Class IIFDA: OngoingSugar Foods Corporation
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026180 records · 4 categoriesSeptember 2026363 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories