Medical DeviceMar 10, 2021
Johnson & Johnson Surgical Vision TECNIS Toric 1-Piece IOL recall — FDA Z-1163-2021
Due to the release of nonconforming Intraocular Lenses (IOLs).
Class IIFDA: TerminatedJohnson & Johnson Surgical Vision 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 110
Records are ordered by the best available source date.
FoodMar 10, 2021
Urban Remedy Organic Almond Maca Almond Milk recall — FDA F-0331-2021
Firm discovered that labeling had been switched for two products on one day of production - undeclared almonds and cashews.
Class IIFDA: TerminatedUrban Remedy
FoodMar 10, 2021
Ferrara Candy Company including Laffy Taffy, Nerds, and SweeTarts candies recall — FDA F-0336-2021
Undeclared ingredients on retail packaging, including but not limited to certified colors Red #40 and Blue #1
Class IIIFDA: TerminatedFerrara Candy Company
FoodMar 10, 2021
Urban Remedy Organic Cacao Mocha Cold Brew Coffee recall — FDA F-0330-2021
Firm discovered that labeling had been switched for two products on one day of production - undeclared almonds and cashews.
Class IIFDA: TerminatedUrban Remedy
FoodMar 10, 2021
Thompson Brands 1 recall — FDA F-0325-2021
Products are potentially contaminated with Salmonella.
Class IFDA: TerminatedThompson Brands LLC
FoodMar 10, 2021
Shenandoah Growers Organic fresh cut basil packaged in plastic clamshell recall — FDA F-0327-2021
Possible contamination with Cyclospora in basil
Class IIFDA: TerminatedShenandoah Growers, Inc.
DrugMar 10, 2021
Daytrana recall — FDA D-0295-2021
Defective Delivery System: Out of specification for mechanical peel.
Class IIFDA: TerminatedNoven Pharmaceuticals Inc.
DrugMar 10, 2021
Daytrana recall — FDA D-0293-2021
Defective Delivery System: Out of specification for mechanical peel.
Class IIFDA: TerminatedNoven Pharmaceuticals Inc.
DrugMar 10, 2021
Daytrana recall — FDA D-0294-2021
Defective Delivery System: Out of specification for mechanical peel.
Class IIFDA: TerminatedNoven Pharmaceuticals Inc.
DrugMar 10, 2021
Metoclopramide Injection USP, 10 mg/2 mL (5 mg/mL), 25x2mL Single Dose Vials recall — FDA D-0297-2021
Chemical contamination; Unknown brown residue adhering to the inside of one vial.
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugMar 10, 2021
Daytrana recall — FDA D-0296-2021
Defective Delivery System: Out of specification for mechanical peel.
Class IIFDA: TerminatedNoven Pharmaceuticals Inc.
DrugMar 10, 2021
Famotidine Tablets USP 40mg, 1,000-count bottles recall — FDA D-0290-2021
Presence of foreign tablets/capsules: Famotidine 20mg and ibuprofen 400mg tablets were found in a lot of famotidine 40mg.
Class IIFDA: TerminatedAurobindo Pharma USA Inc.
DrugMar 10, 2021
Atorvastatin Calcium Tablets, 40mg recall — FDA D-0291-2021
Failed Impurities/Degradation Specifications:presence of ATV cyclo IP and FP, Dihydroxy epoxy and Dieto epoxy impurities
Class IIIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugMar 10, 2021
Jubilant Cadista Pharmaceuticals Methylprednisolone Tablets USP, 4 MG recall — FDA D-0298-2021
Labeling: Illegible label: Customer complaint received of mis-alignment print of the printed dosing instructions on the blister card.
Class IIIFDA: TerminatedJubilant Cadista Pharmaceuticals, Inc.
VehicleMar 10, 2021
Volkswagen Group of air bags recall — NHTSA campaign 21V159000
Volkswagen Group of America, Inc. (Audi) is recalling certain 2021 Audi RS6 Avant, RS7, 2020-2021 A6 Allroad, S6 Sedan, S7, 2019-2021 A6 Sedan, and A7 vehicles. The score line on the…
air bagsVolkswagen Group of America, Inc.
VehicleMar 10, 2021
Ford rear recall — NHTSA campaign 21V154000
Ford Motor Company (Ford) is recalling certain 2020 Lincoln Aviator and Ford Explorer vehicles. The rear lower control arm (RLCA) bolts that attach the rear lower control arms to the wheel…
rearFord Motor Company
VehicleMar 10, 2021
BMW head restraint recall — NHTSA campaign 21V156000
BMW of North America, LLC (BMW) is recalling certain 2021 X5 sDrive40i, X5 xDrive50i, X5 M50i, X5 xDrive45e, 2021 X7 xDrive40i, X7 M50i, and XB7 vehicles. The head restraints on the…
head restraintBMW of North America, LLC
VehicleMar 10, 2021
Ford tires recall — NHTSA campaign 21V155000
Ford Motor Company (Ford) is recalling certain 2018 F-150, 2018-2020 F-250, F-350, and 2019 Escape vehicles equipped with Continental tires. On the affected vehicles, it is possible that…
tiresFord Motor Company
VehicleMar 5, 2021
Atlas sidewall recall — NHTSA campaign 21V142000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2018-2019 Atlas vehicles equipped with Continental tires. On the affected vehicles, it is possible that one or more tires…
sidewallVolkswagen Group of America, Inc.
VehicleMar 4, 2021
Nissan Altima tie rod recall — NHTSA campaign 21V138000
Nissan North America, Inc. (Nissan) is recalling certain 2020-2021 Nissan Altima vehicles. The tie rod ball joint fastener was not tightened properly, which could result in the tie rod ball…
tie rodNissan North America, Inc.
VehicleMar 4, 2021
Kia Motors control unit/module recall — NHTSA campaign 21V137000
Kia Motors America (Kia) is recalling certain 2017-2021 Sportage and Cadenza vehicles. The electrical circuit in the Hydraulic Electronic Control Unit (HECU) may short-circuit, which can…
control unit/moduleKia Motors America
Medical DeviceMar 3, 2021
Medline Industries S-O303000 CONTROL, STAT-SITE B-HB, 2X3ML,1LOW,1HIGH - Product Usage recall — FDA Z-1135-2021
Medline Industries, Inc. is removing specific lots of STAT-Site Controls (Low and High) S-O303000, from the market, due to the product being compromised during shipment.
Class IIIFDA: TerminatedMedline Industries Inc.
Medical DeviceMar 3, 2021
Smiths Medical ASD Tube Tracheostomy and Tube Cuff, Bivona Cuffless Neonatal/Pediatric recall — FDA Z-1145-2021
Smiths Medical became aware that three lot numbers of a specific model of Bivona Cuffless FlexTend" Tracheostomy Tube (model 60PFS45, lots 3991171, 3991172, and 3988103) may have been…
Class IIFDA: TerminatedSmiths Medical ASD Inc.
Medical DeviceMar 3, 2021
Silk Road Medical ENROUTE Transcarotid Stent System REF SR-XXYY-CS recall — FDA Z-1146-2021
Due to complaints received that the tip/nose cone may detach from the Transcarotid Stent System.
Class IIFDA: TerminatedSilk Road Medical 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.