DrugNov 4, 2020
Jarrow Formulas N-A-C recall — FDA D-0302-2021
Mislabeling of SUS (N-A-C Sustain 600 mg 100 tab) with N-A-C N-Acetyl-L-Cysteine 500 mg, 100 cap.
Class IIFDA: TerminatedJarrow Formulas Inc.
Latest records
Latest recalls — page 945
The newest recall records with useful source details are listed here.
VehicleNov 4, 2020
BMW control arm recall — NHTSA campaign 20V678000
BMW of North America, LLC (BMW) is recalling certain 2020 X5 sDrive40i, xDrive40i, X5 M50i, X5M, X7 xDrive40i, X7 M50i, X6 xDrive40i, X6 M50i and X6M vehicles and 2021 X5 xDrive45e…
control armBMW of North America, LLC
VehicleNov 4, 2020
Toyota Motor Engineering & Manufacturing fuel pump recall — NHTSA campaign 20V682000
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2018-2019 4Runner, 2019-2020 Avalon, 2019 Corolla Hatchback, 2017-2019 Highlander, 2018-2020 Camry, 2020 Corolla,…
fuel pumpToyota Motor Engineering & Manufacturing
VehicleOct 29, 2020
General Motors automatic transmission recall — NHTSA campaign 20V668000
General Motors LLC (GM) is recalling certain 2018-2019 Chevrolet Cruze and Buick LaCrosse, 2018-2020 Chevrolet Equinox, Chevrolet Traverse and GMC Terrain, 2018 Chevrolet Malibu, 2019-2020…
automatic transmissionGeneral Motors LLC
Medical DeviceOct 28, 2020
ICU Medical 128" (325 cm) Appx 16.6 ml, 15 Drop Primary Set w/2 MicroClave, Remv 2 Gang recall — FDA Z-0244-2021
Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.
Class IIFDA: TerminatedICU Medical, Inc.
Medical DeviceOct 28, 2020
ICU Medical 10 IN (25cm) APPX 1.5ml EXT w/6-Port NanoClave Manifold, Check Valve. 1 unit per recall — FDA Z-0235-2021
Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.
Class IIFDA: TerminatedICU Medical, Inc.
Medical DeviceOct 28, 2020
ICU Medical 7" (18 cm) Appx 0.32 ml, Smallbore Pressure Infusion (400 psig) Ext Set w/Remv recall — FDA Z-0201-2021
Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.
Class IIFDA: TerminatedICU Medical, Inc.
Medical DeviceOct 28, 2020
ICU Medical 112 IN(284cm) APPX 14.6ml, 15 Drop Set 3 MicroClave, 3-Port NanoClave Manifold recall — FDA Z-0226-2021
Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.
Class IIFDA: TerminatedICU Medical, Inc.
Medical DeviceOct 28, 2020
GE Healthcare Tomographic Imager Combining Emission Computed Tomography With Nuclear recall — FDA Z-0131-2021
Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.
Class IIFDA: TerminatedGE Healthcare, LLC
Medical DeviceOct 28, 2020
ICU Medical 11 IN(28cm)APPX 0.97ml,SMALLBORE SET,NanoClave,6-PORT NanoClave MANIFOLD,BCV.1 recall — FDA Z-0240-2021
Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.
Class IIFDA: TerminatedICU Medical, Inc.
Medical DeviceOct 28, 2020
ICU Medical 5.5" (14 cm) Appx 0.39 ml, Smallbore Trifuse Ext Set w/3 MicroClave Clear recall — FDA Z-0259-2021
Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.
Class IIFDA: TerminatedICU Medical, Inc.
Medical DeviceOct 28, 2020
ICU Medical 54 IN (137 cm) APPX 7.2 ml EXT SET w NanoClave 4-Way Stopcock recall — FDA Z-0216-2021
Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.
Class IIFDA: TerminatedICU Medical, Inc.
Medical DeviceOct 28, 2020
ICU Medical 112 IN (284cm) APPX 14.8ml, 15 Drop Set 3 MicroClave, Remv 3-Port NanoClave recall — FDA Z-0228-2021
Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.
Class IIFDA: TerminatedICU Medical, Inc.
Medical DeviceOct 28, 2020
Siemens Healthcare Diagnostics Atellica IM HER-2/neu (H2n) assay, 50 Test Kit, Catalog No recall — FDA Z-0115-2021
Siemens confirmed that the Upper Limit of Normal (ULN) as claimed in the Instructions for Use (IFU) was no longer achieved. This can potentially result in false positive or false negative…
Class IIFDA: TerminatedSiemens Healthcare Diagnostics, Inc.
Medical DeviceOct 28, 2020
ICU Medical 148 IN (376cm) APPX 18.8 ml, 15 DROP SET, 2 CLAVE, Remv 3 Gang Clave Stopcock.1 recall — FDA Z-0255-2021
Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.
Class IIFDA: TerminatedICU Medical, Inc.
Medical DeviceOct 28, 2020
ICU Medical 124" (315 cm) 60 Drop 150 mL Burette Set (w/Clave, Shut-Off), Remv 2 Gang Clave recall — FDA Z-0260-2021
Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.
Class IIFDA: TerminatedICU Medical, Inc.
Medical DeviceOct 28, 2020
Smith & Nephew TWINFIX ULTRA HA 4.5 W/2 UB BLUE & BLK- Absorbable Suture anchor Product recall — FDA Z-0162-2021
Product packaging improper or incomplete seal of the pouch surrounding the sterile product may result in a breach of the sterile barrier created by the pouch
Class IIFDA: OngoingSmith & Nephew, Inc.
Medical DeviceOct 28, 2020
ICU Medical SURPLUG Nano Connector.1 unit per pouch, 100 multivac pouches per case recall — FDA Z-0280-2021
Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.
Class IIFDA: TerminatedICU Medical, Inc.
Medical DeviceOct 28, 2020
ICU Medical 123 IN (312cm) APPX 16.1 ml, 10 DROP SET w/3 MicroClave, 3-Port NanoClave recall — FDA Z-0222-2021
Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.
Class IIFDA: TerminatedICU Medical, Inc.
Medical DeviceOct 28, 2020
Boston Scientific Opticross 35 15 MHz Peripheral Imaging Catheter 8F (2.74 mm) X 105 cm recall — FDA Z-0181-2021
Opticross 35 Peripheral Imaging Catheter is being recalled because the incremental telescoping length markings near the proximal end of the catheter shaft can flake off when the device is…
Class IIFDA: TerminatedBoston Scientific Corporation
Medical DeviceOct 28, 2020
ICU Medical 78 IN (198cm) APPX 10.0 ml, 20 Drop Set 3-Port NanoClave Manifold, BCV recall — FDA Z-0229-2021
Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.
Class IIFDA: TerminatedICU Medical, Inc.
Medical DeviceOct 28, 2020
Smith & Nephew MICRORAPTOR REGENESORB SUTURE ANCHOR- Absorbable Suture anchor Product recall — FDA Z-0174-2021
Product packaging improper or incomplete seal of the pouch surrounding the sterile product may result in a breach of the sterile barrier created by the pouch
Class IIFDA: OngoingSmith & Nephew, Inc.
Medical DeviceOct 28, 2020
ICU Medical 8" (20 cm) Appx 0.33 ml, Smallbore Ext Set w/MicroClave Clear, NanoClave Clamp recall — FDA Z-0276-2021
Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.
Class IIFDA: TerminatedICU Medical, Inc.
Medical DeviceOct 28, 2020
Smith & Nephew HEALICOIL RSB SA 5.5MM W/1 UT & 1 UB BL- Absorbable Suture anchor Product recall — FDA Z-0173-2021
Product packaging improper or incomplete seal of the pouch surrounding the sterile product may result in a breach of the sterile barrier created by the pouch
Class IIFDA: OngoingSmith & Nephew, Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026111 records · 4 categoriesSeptember 2026364 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