FoodOct 27, 2021
Suntree Snack Foods Mountain Trail Mix, 44 oz recall — FDA F-0062-2022
A customer notified the firm that the product contained glass pieces.
Class IIFDA: TerminatedSuntree Snack Foods, LLC
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 21
Records are ordered by the best available source date.
FoodOct 27, 2021
Farmers' All Natural Creamery Kalona Supernatural Organic Whole Chocolate Milk, Manufactured recall — FDA F-0022-2022
Milk products and shipped without being properly pasteurized.
Class IIFDA: TerminatedFarmers' All Natural Creamery LLC
FoodOct 27, 2021
Chocolate & the Chip The Big Cookie Cake Cookie cakes: 1LB recall — FDA F-0040-2022
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Class IIFDA: TerminatedChocolate and the Chip
FoodOct 27, 2021
Chocolate & the Chip Gluten free original chocolate chip recall — FDA F-0044-2022
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Class IIFDA: TerminatedChocolate and the Chip
FoodOct 27, 2021
Whole Foods Market Everyday Double Crust Apple Pie sold in recall — FDA F-0026-2022
Whole and sliced Apple and Cherry Pies from five stores in the Mid-Atlantic Region contain undeclared milk and egg.
Class IFDA: TerminatedWhole Foods Market Brand 365, LLC
FoodOct 27, 2021
Farmers' All Natural Creamery Kalona Supernatural Organic Half & Half, Manufactured in Iowa recall — FDA F-0021-2022
Milk products and shipped without being properly pasteurized.
Class IIFDA: TerminatedFarmers' All Natural Creamery LLC
FoodOct 27, 2021
Chocolate & the Chip Brown Butter Rice Crispy Treat recall — FDA F-0050-2022
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Class IIFDA: TerminatedChocolate and the Chip
FoodOct 27, 2021
Chocolate & the Chip Peanutbutter Spice Cookies: 4 oz / 114 recall — FDA F-0037-2022
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Class IIFDA: TerminatedChocolate and the Chip
FoodOct 27, 2021
Chocolate & the Chip Boozy Banana Walnut: Cookies: 4 oz / 114 recall — FDA F-0043-2022
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Class IIFDA: TerminatedChocolate and the Chip
DrugOct 27, 2021
Sanitor Cleaning Solutions Foaming Hand Sanitizer, Active Ingredient Benzalkonium chloride recall — FDA D-0018-2022
CGMP Deviations: Use of this product may cause possible infection/ irritation of the skin and/or soft tissues.
Class IIFDA: TerminatedSanitor Corporation
DrugOct 27, 2021
Teva Pharmaceuticals USA AirDuo Digihaler 113/14 recall — FDA D-0021-2022
Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugOct 27, 2021
ACID REDUCER Omeprazole Delayed-Release Capsules, 20 mg* recall — FDA D-0026-2022
CGMP Deviations: Customer complaint for the presence of a staple co-mingled with capsules within the bottle.
Class IIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugOct 27, 2021
Teva Pharmaceuticals USA AirDuo Digihaler 232/14 recall — FDA D-0022-2022
Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugOct 27, 2021
Piramal Critical Care Rocuronium Bromide Injection 50mg/5 mL, 5mL Multi-Dose Vial recall — FDA D-0019-2022
Labeling: Label Lacks Warning or Rx Legend: Finished product did not include the statement on the flip cap vial, "WARNING: PARALYZING AGENT"
Class IIFDA: TerminatedPiramal Critical Care, Inc.
DrugOct 27, 2021
American Health Packaging GlipiZIDE Extended-Release Tablets, 2.5 mg, 30 Tablets recall — FDA D-0020-2022
Failed Dissolution Specifications: results were above specification.
Class IIFDA: TerminatedAmerican Health Packaging
DrugOct 27, 2021
Imipramine Pamoate Capsules 125 mg, 30-count bottle recall — FDA D-0027-2022
Out of specification result observed in a dissolution test at the 9-month long term stability time point.
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
VehicleOct 27, 2021
Palisade fluid recall — NHTSA campaign 21V840000
Hyundai Motor America (Hyundai) is recalling certain 2021 Palisade vehicles. The brake fluid may be contaminated, which can cause the brake master cylinder inner-cup seals to swell, and…
fluidHyundai Motor America
VehicleOct 26, 2021
Rogue Hybrid engine control module (ecu/ecm) recall — NHTSA campaign 21V839000
Nissan North America, Inc. (Nissan) is recalling certain 2017-2019 Rogue Hybrid vehicles. Contact with the Electronic Control Module (ECM) bracket may damage the engine harness, causing a…
engine control module (ecu/ecm)Nissan North America, Inc.
VehicleOct 25, 2021
Tesla curtain recall — NHTSA campaign 21V834000
Tesla, Inc. (Tesla) is recalling certain 2020-2021, 2023 Model 3 vehicles. The left and/or right side curtain air bag may have been improperly secured to the roof rail, which could result…
curtainTesla, Inc.
VehicleOct 25, 2021
Tesla critical fasteners recall — NHTSA campaign 21V835000
Tesla, Inc. (Tesla) is recalling certain 2020-2021 Model Y and 2019-2021 Model 3 vehicles. The front suspension lateral link fasteners may loosen, allowing the lateral link to separate from…
critical fastenersTesla, Inc.
Medical DeviceOct 20, 2021
smiths medical medex HemoDraw Plus Closed Blood Sampling Set with LogiCal Pressure recall — FDA Z-0093-2022
Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets.
Class IIFDA: TerminatedSmiths Medical ASD Inc.
Medical DeviceOct 20, 2021
Philips recall — FDA Z-0080-2022
Customers were not notified of previous recalls associated with various defibrillator models.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceOct 20, 2021
Bio-Rad Laboratories BioPlex 2200 ANA Screen Control Set, REF: 663-1131 incompatible with recall — FDA Z-0082-2022
A new lot of ANA screen control and any subsequent control lots are incompatible with older lot numbers of ANA calibrators and ANA reagent packs.
Class IIFDA: TerminatedBio-Rad Laboratories, Inc.
Medical DeviceOct 20, 2021
Flower Drill Bit Kit 2.7mm- The Drill Bit Kit, 2.7mm (DBK 027) is intended to be used with recall — FDA Z-0113-2022
Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
Class IIFDA: TerminatedFlower Orthopedics Corporation
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.