Medical DeviceSep 2, 2020
Datascope Intra-Aortic Ballon Catheters (IABs)-TRANS-RAY PLUS 7.5Fr 35cc IAB (Japan) Kit recall — FDA Z-2843-2020
Potential Endotoxin Contamination
Class IIFDA: OngoingDatascope Corporation
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 55
Records are ordered by the best available source date.
Medical DeviceSep 2, 2020
Ortho Clinical Diagnostics VITROS XT7600 Integrated System, Product code 6844461 recall — FDA Z-2879-2020
When processing MicroSlides, slides that utilize Slot 18 in the CM rotor may be mis-positioned. As a result, certain VITROS MicroSlides may produce erroneous results.
Class IIFDA: TerminatedOrtho Clinical Diagnostics
Medical DeviceSep 2, 2020
Biosense Webster (israel) CARTO 3 System (Software Version V7.1.80), CARTO VISITAG Module recall — FDA Z-2880-2020
Software defect may result in disapperance of tag sites during recalculation and lead to additional ablation sites. This may lead to prolongation of the procedure and, in extremely rare…
Class IIFDA: TerminatedBiosense Webster (israel), Ltd.
Medical DeviceSep 2, 2020
Ortho-Clinical Diagnostics VITROS XT Chemistry Products TBIL-ALKP Slides recall — FDA Z-2875-2020
Etrombopag Interference for VITROS Chemistry Products: TBIL Slides, VITROS BuBc Slides and VITROS XT TBIL-ALKP Slides
Class IIFDA: TerminatedOrtho-Clinical Diagnostics
Medical DeviceSep 2, 2020
Datascope Intra-Aortic Ballon Catheters (IABs)-Trans-Ray 7Fr 40cc IAB (Japan) - Product recall — FDA Z-2842-2020
Potential Endotoxin Contamination
Class IIFDA: OngoingDatascope Corporation
Medical DeviceSep 2, 2020
Siemens Medical Solutions USA Cios Spin, Image-Intensified Fluoroscopic X-Ray System The recall — FDA Z-2888-2020
Siemens has become aware of a hardware error which affects Cios Spin and Cios Alpha systems after the previous repair of the X-ray Generator with an integrated Energy Storage Unit (ESU).
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Medical DeviceSep 2, 2020
Neurovision Medical Products Cobra x5 2-Ch EMG ET Tube, 7.0mm, REF: LTE700DCM-5, Rx Only recall — FDA Z-2907-2020
The electrode insulating material on the Cobra EMG ET tube used for continuous EMG monitoring may soften over time so that it may be more susceptible to damage by scratching or bending,…
Class IIFDA: TerminatedNeurovision Medical Products Inc.
Medical DeviceSep 2, 2020
Neurovision Medical Products Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube, 8.0 recall — FDA Z-2902-2020
The electrode insulating material on the Cobra EMG ET tube used for continuous EMG monitoring may soften over time so that it may be more susceptible to damage by scratching or bending,…
Class IIFDA: TerminatedNeurovision Medical Products Inc.
Medical DeviceSep 2, 2020
Karl Storz Endoscopy Flexible DCI Intubation Fiberscope, Part: 11302BDD2, with Instruction recall — FDA Z-2895-2020
Updated sterilization instructions are being provided to ensure 1) a specific sterilization tray is not used, and 2) ethylene oxide sterilization is never used on certain reusable flexible…
Class IIFDA: OngoingKarl Storz Endoscopy
Medical DeviceSep 2, 2020
Karl Storz Endoscopy Flexible Intubation Fiberscope, Part: 11301BN1, with Instruction recall — FDA Z-2892-2020
Updated sterilization instructions are being provided to ensure 1) a specific sterilization tray is not used, and 2) ethylene oxide sterilization is never used on certain reusable flexible…
Class IIFDA: OngoingKarl Storz Endoscopy
Medical DeviceSep 2, 2020
Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 34cc IAB Kit P/N recall — FDA Z-2839-2020
Potential Endotoxin Contamination
Class IIFDA: OngoingDatascope Corporation
FoodSep 2, 2020
Thomson International Red onions recall — FDA F-1272-2020
Traceback investigation into an outbreak of Salmonella Newport illnesses found red onions to be a suspect vehicle for the outbreak. After notification from FDA, firm initiated a recall.
Class IFDA: TerminatedThomson International, Inc.
FoodSep 2, 2020
Thomson International Sweet Yellow onions recall — FDA F-1275-2020
Traceback investigation into an outbreak of Salmonella Newport illnesses found red onions to be a suspect vehicle for the outbreak. After notification from FDA, firm initiated a recall.
Class IFDA: TerminatedThomson International, Inc.
FoodSep 2, 2020
Emerald Fruit & Produce Onions Yellow Whole Dry 5 lb recall — FDA F-1270-2020
Processed onions products are recalled due to a potential contamination with Salmonella Newport. Onions were supplied from Thomson International Inc.
Class IFDA: TerminatedEmerald Fruit & Produce Inc.
FoodSep 2, 2020
Emerald Fruit & Produce M60058CS Onions White Diced sold by pound for foodservice use recall — FDA F-1268-2020
Processed onions products are recalled due to a potential contamination with Salmonella Newport. Onions were supplied from Thomson International Inc.
Class IFDA: TerminatedEmerald Fruit & Produce Inc.
FoodSep 2, 2020
Fantis Foods California 25 oz recall — FDA F-1349-2020
Individual product packaging does state Whey in ingredients but does not declare Milk as an allergen
Class IIFDA: TerminatedFantis Foods California, Inc.
FoodSep 2, 2020
Progressive Produce Yellow Onions recall — FDA F-1256-2020
Onions supplied by Thomson Onions were distributed for retail sale.
Class IFDA: TerminatedProgressive Produce LLC
FoodSep 2, 2020
Wegmans Chicken Cutlet recall — FDA F-1293-2020
Products are potentially contaminated with Listeria monocytogenes.
Class IIIFDA: TerminatedWegmans Food Markets, Inc.
FoodSep 2, 2020
Almark Foods ORGANIC VALLEY EGG BITES feta & chives NET WT 4 OZ recall — FDA F-1363-2020
The firm was notified by their customer that the product is missing the back panel containing the ingredient, nutrition and allergen statements. Product contains eggs and milk.
Class IIFDA: TerminatedAlmark Foods
FoodSep 2, 2020
Emerald Fruit & Produce M60025CS Onions Yellow Diced sold by pound for foodservice use recall — FDA F-1261-2020
Processed onions products are recalled due to a potential contamination with Salmonella Newport. Onions were supplied from Thomson International Inc.
Class IFDA: TerminatedEmerald Fruit & Produce Inc.
FoodSep 2, 2020
Emerald Fruit & Produce Onions Red Whole Dry 5 lb recall — FDA F-1265-2020
Processed onions products are recalled due to a potential contamination with Salmonella Newport. Onions were supplied from Thomson International Inc.
Class IFDA: TerminatedEmerald Fruit & Produce Inc.
FoodSep 2, 2020
Thomson International White onions recall — FDA F-1274-2020
Traceback investigation into an outbreak of Salmonella Newport illnesses found red onions to be a suspect vehicle for the outbreak. After notification from FDA, firm initiated a recall.
Class IFDA: TerminatedThomson International, Inc.
FoodSep 2, 2020
Emerald Fruit & Produce M60022CS Onions Red Diced sold by pound for foodservice use recall — FDA F-1264-2020
Processed onions products are recalled due to a potential contamination with Salmonella Newport. Onions were supplied from Thomson International Inc.
Class IFDA: TerminatedEmerald Fruit & Produce Inc.
FoodSep 2, 2020
Emerald Fruit & Produce M60064CS Onions White Sliced sold by pound for foodservice use recall — FDA F-1267-2020
Processed onions products are recalled due to a potential contamination with Salmonella Newport. Onions were supplied from Thomson International Inc.
Class IFDA: TerminatedEmerald Fruit & Produce 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.