DrugAug 12, 2020
MICHIGAN HERBAL REMEDIES Tasty Drops, Hemp Oil Extract, Vanilla, 1500MG CBD,1 FL recall — FDA D-1477-2020
Chemical contamination: product contains elevated levels of undeclared lead.
Class IFDA: CompletedMICHIGAN HERBAL REMEDIES
Monthly breakdown
2020 recalls by month
Select a month to review the recall records reported during that period.
December 2020315 records · 4 categoriesNovember 2020241 records · 4 categoriesOctober 2020416 records · 4 categoriesSeptember 2020371 records · 4 categoriesAugust 2020245 records · 4 categoriesJuly 2020442 records · 4 categoriesJune 2020342 records · 4 categoriesMay 2020315 records · 4 categoriesApril 2020422 records · 4 categoriesMarch 2020368 records · 4 categoriesFebruary 2020551 records · 4 categoriesJanuary 2020224 records · 4 categories
2020 recalls — page 65
Records are ordered by the best available source date.
DrugAug 12, 2020
MICHIGAN HERBAL REMEDIES Made by Hemp 1000MG Hemp Extract, French Vanilla, 1 OZ (30 ML) recall — FDA D-1451-2020
Chemical contamination: product contains elevated levels of undeclared lead.
Class IFDA: CompletedMICHIGAN HERBAL REMEDIES
DrugAug 12, 2020
MICHIGAN HERBAL REMEDIES BC Hemp Co., Full Spectrum Hemp Extract, CBD Oil, Berry Blast recall — FDA D-1457-2020
Chemical contamination: product contains elevated levels of undeclared lead.
Class IFDA: CompletedMICHIGAN HERBAL REMEDIES
VehicleAug 10, 2020
F-150 starter motor recall — NHTSA campaign 20V467000
Ford Motor Company (Ford) is recalling certain 2020 F-150 vehicles. An incorrect attachment nut may have been used to attach the battery positive (B+) power supply cable to the starter…
starter motorFord Motor Company
Medical DeviceAug 5, 2020
Steris InnoWave Sonic Irrigator, There are currently six models recall — FDA Z-2700-2020
A recent FDA inspection at the firm identified that the foil test performed during installation of the device does not have clear acceptance criteria.
Class IIFDA: TerminatedSteris Corporation
Medical DeviceAug 5, 2020
TELEFLEX MEDICAL Rusch Greenlite Product Code: 004550004 GTIN: 14026704663085 (each) recall — FDA Z-2728-2020
Breaking at the point of a welded joint
Class IIFDA: TerminatedTELEFLEX MEDICAL Inc.
Medical DeviceAug 5, 2020
TELEFLEX MEDICAL Rusch Greenlite Product Code: 004551002 GTIN: 14026704663115 (each) recall — FDA Z-2729-2020
Breaking at the point of a welded joint
Class IIFDA: TerminatedTELEFLEX MEDICAL Inc.
Medical DeviceAug 5, 2020
Shanghai United Imaging Healthcare Co Computed Tomography X-ray System recall — FDA Z-2705-2020
The metal edge overlap of the mylar strip in the gantry was uneven, which may create a sharp edge.
Class IIFDA: OngoingShanghai United Imaging Healthcare Co., Ltd.
Medical DeviceAug 5, 2020
Medline Industries ClearPro T-Piece Closed Suction Catheter, Model DYNCPTP14, 14 Fr 21.3 IN recall — FDA Z-2724-2020
There are reports of the suction catheter coming apart from the device assembly during use.
Class IIFDA: OngoingMedline Industries Inc.
Medical DeviceAug 5, 2020
Hill-Rom Centrella Smart+ Bed, Catalog No recall — FDA Z-2738-2020
Affected beds may have screws installed that do not meet material tensile strength requirements. Failure of this screw could result in serious patient or user injury.
Class IIFDA: TerminatedHill-Rom, Inc.
Medical DeviceAug 5, 2020
TELEFLEX MEDICAL Rusch Greenlite Product Code: 004551003 GTIN: 14026704663122 (each) recall — FDA Z-2730-2020
Breaking at the point of a welded joint
Class IIFDA: TerminatedTELEFLEX MEDICAL Inc.
Medical DeviceAug 5, 2020
Abbott Gmbh & Co. KG Alinity ci series System Control Module (SCM) recall — FDA Z-2701-2020
Quality Control results were not properly evaluated for QC failures.
Class IIFDA: TerminatedAbbott Gmbh & Co. KG
Medical DeviceAug 5, 2020
Synthes MatrixNEURO Screws - Product Usage: The intended use for this device is in fixation recall — FDA Z-2698-2020
One lot of MatrixNEURO 5mm screws was packaged in a body clip etched "4", which indicated a 4mm screw. The outer package labeling correctly identifies a 5mm screw, but the body clop…
Class IIFDA: TerminatedSynthes, Inc.
Medical DeviceAug 5, 2020
TELEFLEX MEDICAL Rusch Greenlite Product Code: 004551035 GTIN:7290102156443 (each) - Product recall — FDA Z-2732-2020
Breaking at the point of a welded joint
Class IIFDA: TerminatedTELEFLEX MEDICAL Inc.
Medical DeviceAug 5, 2020
Shanghai United Imaging Healthcare Co Computed Tomography X-ray System recall — FDA Z-2703-2020
The metal edge overlap of the mylar strip in the gantry was uneven, which may create a sharp edge.
Class IIFDA: OngoingShanghai United Imaging Healthcare Co., Ltd.
Medical DeviceAug 5, 2020
Arthrex Sterile Low Profile Screw, Titanium, 6.7 x 65mm Part Number: AR-8967-2865S - Product recall — FDA Z-2733-2020
Screws provided in packaging are 5mm shorter than intended
Class IIFDA: TerminatedArthrex, Inc.
Medical DeviceAug 5, 2020
Resource Optimization & Innovation regard Migrating Indicator, STEAM Migrating Indicator recall — FDA Z-2699-2020
The firm received reports from customer that the Regard Migrating Indicator shown malfunctions and does not go into the "accept" window at the time of use.
Class IIFDA: TerminatedResource Optimization & Innovation LLC
Medical DeviceAug 5, 2020
Smith & Nephew T-F1X0 RCG Drill Pac, 2 mm Drill & (2) Sleeves - Product Usage: indicated for recall — FDA Z-2702-2020
The T-Fix sterile package contains only one sleeve instead of two, The device will not perform as intended for the second bone tunnel due to the absence of thesleeve
Class IIFDA: OngoingSmith & Nephew, Inc.
Medical DeviceAug 5, 2020
Richard Wolf GmbH Tube Set for TEM - Product Usage: Transanal Endoscopic Microsurgery (TEM) recall — FDA Z-2706-2020
Tube material of a smaller diameter was used.
Class IIFDA: TerminatedRichard Wolf GmbH
Medical DeviceAug 5, 2020
Medline Industries ClearPro Trach T-Piece Closed Suction Catheter, Model DYNCPTP14T, 14 Fr recall — FDA Z-2725-2020
There are reports of the suction catheter coming apart from the device assembly during use.
Class IIFDA: OngoingMedline Industries Inc.
Medical DeviceAug 5, 2020
TELEFLEX MEDICAL Rusch Greenlite Product Code: 0004550003 GTIN: 14026704663078 (each) recall — FDA Z-2727-2020
Breaking at the point of a welded joint
Class IIFDA: TerminatedTELEFLEX MEDICAL Inc.
Medical DeviceAug 5, 2020
Shanghai United Imaging Healthcare Co Computed Tomography X-ray System recall — FDA Z-2704-2020
The metal edge overlap of the mylar strip in the gantry was uneven, which may create a sharp edge.
Class IIFDA: OngoingShanghai United Imaging Healthcare Co., Ltd.
Medical DeviceAug 5, 2020
Synthes Produktions GmbH MatrixMIDFACE Screws - Product Usage: The intended use for this recall — FDA Z-2739-2020
One lot of MatrixMIDFACE Emergency Screw 1.8mm, self-tapp, L 12mm, in Clip was packaged with a body clip etched with a 3 (representing 3mm) when it should have been packaged with body clip…
Class IIFDA: TerminatedSynthes Produktions GmbH
Medical DeviceAug 5, 2020
Hill-Rom Progressa Bed, Catalog No recall — FDA Z-2737-2020
Affected beds may have screws installed that do not meet material tensile strength requirements. Failure of this screw could result in serious patient or user injury.
Class IIFDA: TerminatedHill-Rom, Inc.
About the 2020 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.