FoodMar 31, 2021
El Abuelito Cheese Requeson/Ricotta, sold under the following brands and recall — FDA F-0346-2021
Product may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedEl Abuelito Cheese, Inc.
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 104
Records are ordered by the best available source date.
FoodMar 31, 2021
Western Mixers Produce & Nuts Gelson's Yogurt Raisins, Plastic Clamshell Container NET WT 14 recall — FDA F-0353-2021
Gelson's Yogurt Raisins may contain yogurt peanuts.
Class IFDA: TerminatedWestern Mixers Produce & Nuts, Inc.
FoodMar 31, 2021
Taylor Farms Northwest Item #140946, Chicken Salad Croissant Sandwich, Refrigerated recall — FDA F-0350-2021
Undeclared Soy Lecithin. Croissant contains Margarine (Soy Lecithin) but finished Croissant sandwich product label does not declare Soy Lecithin.
Class IIFDA: TerminatedTaylor Farms Northwest, LLC
FoodMar 31, 2021
Taylor Farms Northwest Item #140952, Tuna Salad Croissant Sandwich, Refrigerated recall — FDA F-0351-2021
Undeclared Soy Lecithin. Croissant contains Margarine (Soy Lecithin) but finished Croissant sandwich product label does not declare Soy Lecithin.
Class IIFDA: TerminatedTaylor Farms Northwest, LLC
FoodMar 31, 2021
Taylor Farms Northwest Item #140804, Egg Salad Croissant Sandwich, Refrigerated recall — FDA F-0349-2021
Undeclared Soy Lecithin. Croissant contains Margarine (Soy Lecithin) but finished Croissant sandwich product label does not declare Soy Lecithin.
Class IIFDA: TerminatedTaylor Farms Northwest, LLC
FoodMar 31, 2021
El Abuelito Cheese Quesillo sold under the following brands and container sizes recall — FDA F-0347-2021
Product may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedEl Abuelito Cheese, Inc.
FoodMar 31, 2021
Lehi Valley Trading Co Buc-ee's Butter Toffee Almonds, 12 oz., packaged in clear zip recall — FDA F-0352-2021
Butter Toffee Peanuts mislabeled as Butter Toffee Almonds
Class IIFDA: TerminatedLehi Valley Trading Co, Inc.
FoodMar 31, 2021
El Abuelito Cheese Quseo Fresco sold under the following brands and container recall — FDA F-0345-2021
Product may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedEl Abuelito Cheese, Inc.
DrugMar 31, 2021
Adams.Secret.co Adam's Secret Extra Strength 1500, 800 mg, 10 count blister packs recall — FDA D-0310-2021
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and sildenafil.
Class IFDA: TerminatedAdams.Secret.co
DrugMar 31, 2021
Golden State Medical Supply Omeprazole Delayed Release Capsules, USP, 20 mg, 1000-count recall — FDA D-0312-2021
Failed Impurities/Degradation Specifications: Out of Specification results obtained for unknown impurities during stability testing by manufacturer
Class IIFDA: TerminatedGolden State Medical Supply Inc.
DrugMar 31, 2021
Adams.Secret.co Adam's Secret Extra Strength 3000, 840 mg, 10 count blister packs recall — FDA D-0311-2021
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and sildenafil.
Class IFDA: TerminatedAdams.Secret.co
DrugMar 31, 2021
SODIUM CHLORIDE 0.9% SODIUM CHLORIDE Irrigation, USP 1000 mL Semi-Rigid Bottle recall — FDA D-0313-2021
Presence of particulate matter.one confirmed customer report of particulate matter within two semi-rigid bottles identified prior to use
Class IIFDA: TerminatedICU Medical Inc.
VehicleMar 25, 2021
Chevrolet Tahoe rear/other recall — NHTSA campaign 21V210000
General Motors, LLC (GM) is recalling certain 2021 Chevrolet Tahoe vehicles. The second-row center seat belt latch may be trapped beneath the trim bezel and therefore inaccessible. As such,…
rear/otherGeneral Motors, LLC
VehicleMar 25, 2021
Honda fuel pump recall — NHTSA campaign 21V215000
Honda (American Honda Motor Co.) is recalling certain 2019-2020 Acura MDX, MDX Sport Hybrid, RDX, TLX, Honda Accord, Civic Hatchback, Insight, 2019 Acura ILX, Honda Accord Hybrid, Civic…
fuel pumpHonda (American Honda Motor Co.)
Medical DeviceMar 24, 2021
Cordis PRECISE PRO RX CAROTID STENT implant system, Product Codes: PC0520RXC, PC0530RXC recall — FDA Z-1257-2021
Distal tip may become separated from the lumen wire in specific lots.
Class IFDA: CompletedCordis Corporation
Medical DeviceMar 24, 2021
Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000V Catheterization Table CAT-880B recall — FDA Z-1269-2021
System table may tilt because the bolts that fasten the vertical column and the table top tilting drive unit may become loose.
Class IIFDA: OngoingCanon Medical System, USA, Inc.
Medical DeviceMar 24, 2021
Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000C Catheterization Table CAT-880B recall — FDA Z-1270-2021
System table may tilt because the bolts that fasten the vertical column and the table top tilting drive unit may become loose.
Class IIFDA: OngoingCanon Medical System, USA, Inc.
Medical DeviceMar 24, 2021
Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000F Catheterization Table CAT-880B recall — FDA Z-1271-2021
System table may tilt because the bolts that fasten the vertical column and the table top tilting drive unit may become loose.
Class IIFDA: OngoingCanon Medical System, USA, Inc.
Medical DeviceMar 24, 2021
Merit Medical Systems HeartSpan Transseptal Needles Catalog No recall — FDA Z-1262-2021
The labeled needle tip curvature of specific lots of transseptal needles may not match the actual needle tip curvature. In the event that the incorrect needle is unknowingly used, an…
Class IIFDA: TerminatedMerit Medical Systems, Inc.
Medical DeviceMar 24, 2021
R & D Systems Quantikine IVD Human sTfR Immunoassay recall — FDA Z-1255-2021
R&D Systems, Inc. received two complaints that the standard signal was low and controls were not within the specification range provided with the kit. Investigation confirmed low standard…
Class IIFDA: TerminatedR & D Systems, Inc.
Medical DeviceMar 24, 2021
Philips Incisive CT Computed Tomography X-ray System Model: 728143 recall — FDA Z-1265-2021
Actuators in the Incisive gantry could result in the gantry failure to self-lock if both of the 2 sides actuators fail. In some cases in systems with affected components, the gantry may…
Class IIFDA: TerminatedPhilips North America LLC
Medical DeviceMar 24, 2021
Imactis Impactis NaviKit-stereotaxic accessory for Computed Tomography systems Reference # recall — FDA Z-1264-2021
Defect in the mechanical assembly of the needle holder contained in the navigation kit. One of the 2 jaws of the needle holder does not provide gripping functionality; if the defect is not…
Class IIFDA: TerminatedImactis
Medical DeviceMar 24, 2021
Siemens Medical Solutions USA Software versions syngo.CT VA30A_SP2 or syngo.CT VA30A_SP2a in recall — FDA Z-1253-2021
SOMATOM systems-issues in with software syngo.CT VA30A_SP2 or syngo.CT VA30A_SP2a, may result in sporadic problems causing scanning workflow interruptions and unexpected user notifications.…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Medical DeviceMar 24, 2021
Medtronic Custom Pack EVNP Clinical with AP40 1/B (PERFUSION M448036B 1/B) recall — FDA Z-1194-2021
Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.
Class IFDA: TerminatedMedtronic Perfusion Systems
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.