FoodApr 28, 2021
Amra Services Glutenull Goji Berries & Chocolate Cookies, packaged in a recall — FDA F-0435-2021
Undeclared milk.
Class IFDA: TerminatedAmra Services Ltd.
Monthly breakdown
2021 recalls by month
Select a month to review the recall records reported during that period.
December 2021194 records · 4 categoriesNovember 2021210 records · 4 categoriesOctober 2021342 records · 4 categoriesSeptember 2021300 records · 4 categoriesAugust 2021279 records · 4 categoriesJuly 2021251 records · 4 categoriesJune 2021361 records · 4 categoriesMay 2021226 records · 4 categoriesApril 2021279 records · 4 categoriesMarch 2021241 records · 4 categoriesFebruary 2021320 records · 4 categoriesJanuary 2021226 records · 4 categories
2021 recalls — page 94
Records are ordered by the best available source date.
FoodApr 28, 2021
Jansala & Foods Thai Home brand Panang Curry Paste packaged in glass jars recall — FDA F-0443-2021
Elevated water activity level in shelf-stable products.
Class IIIFDA: TerminatedJansala & Foods LLC
FoodApr 28, 2021
Tropicana Products KeVita Cucumber Rosemary recall — FDA F-0434-2021
Firm initiated a recall because of mislabeling of bottled product inside case.
Class IIFDA: TerminatedTropicana Products, Inc.
DrugApr 28, 2021
Edge Pharma Betadine (Povidone-Iodine) 5%, 0.5mL per syringe Single Use Syringe recall — FDA D-0335-2021
Defective container; syringe content migrating past the seal of the plunger may cause a lack of assurance of sterility
Class IIFDA: TerminatedEdge Pharma, LLC
DrugApr 28, 2021
Minivelle recall — FDA D-0336-2021
Defective Delivery System: Out of specification for release rate testing and shear, an attribute related to the adhesive properties of the transdermal patches. As a result, patients could…
Class IIFDA: TerminatedNoven Pharmaceuticals Inc.
DrugApr 28, 2021
Estradiol Transdermal System Delivers 0.0375 mg/day, 8 Systems/box recall — FDA D-0337-2021
Defective Delivery System: Out of specification for release rate testing and shear, an attribute related to the adhesive properties of the transdermal patches. As a result, patients could…
Class IIFDA: TerminatedNoven Pharmaceuticals Inc.
VehicleApr 28, 2021
Elantra recliner recall — NHTSA campaign 21V302000
Hyundai Motor America (Hyundai) is recalling certain 2021 Elantra vehicles. The driver and front passenger seat back recliners may have been improperly welded.
reclinerHyundai Motor America
VehicleApr 28, 2021
Hyundai Motor engine recall — NHTSA campaign 21V301000
Hyundai Motor America (Hyundai) is recalling certain 2019-2020 Elantra, 2019-2021 Kona and Veloster vehicles equipped with 2.0L Nu MPI engines. The piston oil rings may not have been…
engineHyundai Motor America
VehicleApr 26, 2021
Volkswagen Group of non-powered axle recall — NHTSA campaign 21V295000
Volkswagen Group of America, Inc. (Audi) is recalling certain 2021 Q7, Q8, Q5 Sportback, SQ5 Sportback, RS6 Avant, RS7, RS Q8, 2020-2021 Audi S6 sedan, Q5, A8, S8, A7, A6 Allroad, A5…
non-powered axleVolkswagen Group of America, Inc.
VehicleApr 22, 2021
Rogue caliper recall — NHTSA campaign 21V286000
Nissan North America, Inc. (Nissan) is recalling certain 2021 Rogue vehicles. The rear left and/or right brake caliper assemblies may be missing an internal bushing, allowing the O-ring…
caliperNissan North America, Inc.
Medical DeviceApr 21, 2021
Siemens Healthcare Diagnostics ADVIA 2120 Dual Aspirate Autosampler (SMN 10313419) - US recall — FDA Z-1387-2021
Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceApr 21, 2021
Siemens Healthcare Diagnostics ADVIA 2120i Refurb Single Aspirate (SMN 11314044) - US recall — FDA Z-1392-2021
Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceApr 21, 2021
Siemens Healthcare Diagnostics ADVIA 2120 REFURB SAA AUTOSAMPLER (SMN 10374453) - US recall — FDA Z-1388-2021
Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceApr 21, 2021
Siemens Healthcare Diagnostics ADVIA 2120i Dual Aspirate Autosampler (SMN 10285573) - US recall — FDA Z-1391-2021
Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceApr 21, 2021
Becton Dickinson & Co BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended for recall — FDA Z-1416-2021
BioGX SARS-CoV-2 Reagents for BD MAX" System rehydration buffer tubes were not adequately sealed causing some tubes to be partially filled or empty upon use. A partially filled or empty…
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceApr 21, 2021
Remel Haemophilus Test Medium (150 mm) 10/PK, REF 04033 Remel Haemophilus Test Medium (HTM) recall — FDA Z-1424-2021
When tested with H. influenza ATCC 49247 and ATCC 49766 both organisms may exhibit lighter than normal growth making zones difficult to measure.
Class IIFDA: OngoingRemel Inc.
Medical DeviceApr 21, 2021
Boston Scientific MAMBA Microcatheter recall — FDA Z-1430-2021
The firm initiated a removal of certain batches of MAMBA 135 and MAMBA Flex 135 Microcatheters due to incorrect labeling and packaging.
Class IIFDA: TerminatedBoston Scientific Corporation
Medical DeviceApr 21, 2021
Arthrex Tibial Opening Wedge Osteotomy Plate, Titanium, 15.0 mm - Product Usage: use in recall — FDA Z-1380-2021
It was discovered that five AR-13200ST-15.0 parts were processed as AR-13200T-15.0 parts.
Class IIFDA: TerminatedArthrex, Inc.
Medical DeviceApr 21, 2021
Siemens Healthcare Diagnostics ADVIA 2120i with Single Aspirate Autosampler (SMN 10488923) recall — FDA Z-1400-2021
Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceApr 21, 2021
Siemens Healthcare Diagnostics ADVIA 2120 REFURB DAA AUTOSAMPLER (SMN 10374454) - US recall — FDA Z-1389-2021
Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceApr 21, 2021
EOS Imaging The EOSedge system may acquire two simultaneous orthogonal planar images for a recall — FDA Z-1415-2021
Inadequate images resizing and 2D measurement errors may occur when biplanar acquisition has been performed with patient orientation different from AP (Antero-Posterior).
Class IIFDA: TerminatedEOS Imaging
Medical DeviceApr 21, 2021
Krishe Disposable Sampling Tube, REF VSM01, Contents: Transport Media - 50, Nasal Swab - 50 recall — FDA Z-1420-2021
Verification and validation of the virus transport medium tubes was not provided to FDA prior to sale and marketing
Class IIFDA: TerminatedKrishe Inc.
Medical DeviceApr 21, 2021
Covidien Signia Grey Small Diameter Curved Tip Intelligent Reload 30 mm Vascular 8 mm recall — FDA Z-1384-2021
Potential for the device safety interlock to fail. The safety interlock prevents an empty single-use reload from being erroneously fired a second time. If the safety interlock fails and the…
Class IIFDA: TerminatedCovidien, LP
Medical DeviceApr 21, 2021
Siemens Healthcare Diagnostics ADVIA 2120 Dual Aspirate Autosampler (SMN 10313419) - OUS recall — FDA Z-1397-2021
Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
About the 2021 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.