FoodJan 27, 2021
JTM Provisions Co JTM FOOD GROUP brand READY TO EAT WHITE CHEDDAR MACARONI & recall — FDA F-0216-2021
Possible metal shavings.
Class IIFDA: TerminatedJTM Provisions Co Inc.
January 2021 recalls — page 2
These records include useful source details for the selected month.
FoodJan 27, 2021
GH Foods CA Spinach and Basil Pasta Salad Kit 2/5 lb recall — FDA F-0213-2021
Contain Eggs was not listed on scale label printed at retail stores. Label does state that the product May contain any of the eight allergen that are listed out on the label,
Class IFDA: TerminatedGH Foods CA LLC
FoodJan 27, 2021
Piping Rock Health Products FITNESS LABS***Organic***Coconut Oil***Extra Virgin***16 fl recall — FDA F-0226-2021
Product is potentially contaminated with mold.
Class IIFDA: TerminatedPiping Rock Health Products
FoodJan 27, 2021
GH Foods CA Italian Pasta Salad Kit 2/5 lb recall — FDA F-0211-2021
Contain Eggs was not listed on scale label printed at retail stores. Label does state that the product May contain any of the eight allergen that are listed out on the label,
Class IFDA: TerminatedGH Foods CA LLC
FoodJan 27, 2021
GH Foods CA Smoked Mozzarella Pasta Salad Kit 2/5 lb recall — FDA F-0212-2021
Contain Eggs was not listed on scale label printed at retail stores. Label does state that the product May contain any of the eight allergen that are listed out on the label,
Class IFDA: TerminatedGH Foods CA LLC
FoodJan 27, 2021
GH Foods CA Asian Noodle Salad Kit 2/5 lb recall — FDA F-0209-2021
Contain Eggs was not listed on scale label printed at retail stores. Label does state that the product May contain any of the eight allergen that are listed out on the label,
Class IFDA: TerminatedGH Foods CA LLC
FoodJan 27, 2021
GH Foods CA Pesto Pasta Salad Kit 2/5 lb recall — FDA F-0210-2021
Contain Eggs was not listed on scale label printed at retail stores. Label does state that the product May contain any of the eight allergen that are listed out on the label,
Class IFDA: TerminatedGH Foods CA LLC
FoodJan 27, 2021
GH Foods CA Spinach and Orzo Pasta Kit 2/5 lb recall — FDA F-0214-2021
Contain Eggs was not listed on scale label printed at retail stores. Label does state that the product May contain any of the eight allergen that are listed out on the label,
Class IFDA: TerminatedGH Foods CA LLC
FoodJan 27, 2021
JR Simplot Company - Headquarters SPUD-QUEEN LATTICE CUT - SKIN ON FROZEN POTATOES, master recall — FDA F-0208-2021
Undeclared wheat.
Class IFDA: TerminatedJR Simplot Company - Headquarters
DrugJan 27, 2021
Complete Pharmacy and Medical Solutions, LLC HUMAN CHORIONIC GONADOTROPIN 5,000 IU per vial recall — FDA D-0236-2021
CGMP deviations: Lack of potency testing.
Class IIFDA: TerminatedComplete Pharmacy and Medical Solutions, LLC.
DrugJan 27, 2021
Complete Pharmacy and Medical Solutions, LLC HUMAN CHORIONIC GONADOTROPIN 6,000 IU per vial recall — FDA D-0235-2021
CGMP deviations: Lack of potency testing.
Class IIFDA: TerminatedComplete Pharmacy and Medical Solutions, LLC.
DrugJan 27, 2021
Edge Pharma Ceftazidime Sterile Ophthalmic Solution for Injection Preservative Free 11.25mg recall — FDA D-0238-2021
Lack of Assurance of Sterility; the media used to conduct post-compounding sterility testing for the Methotrexate product was expired.
Class IIFDA: TerminatedEdge Pharma, LLC
DrugJan 27, 2021
Complete Pharmacy and Medical Solutions, LLC HUMAN CHORIONIC GONADOTROPIN 11,000 IU per vial recall — FDA D-0234-2021
CGMP deviations: Lack of potency testing.
Class IIFDA: TerminatedComplete Pharmacy and Medical Solutions, LLC.
DrugJan 27, 2021
Complete Pharmacy and Medical Solutions, LLC HUMAN CHORIONIC GONADOTROPIN 1,250 IU per vial recall — FDA D-0237-2021
CGMP deviations: Lack of potency testing.
Class IIFDA: TerminatedComplete Pharmacy and Medical Solutions, LLC.
VehicleJan 27, 2021
Volkswagen Group of critical fasteners recall — NHTSA campaign 21V027000
Volkswagen Group of America, Inc. (Audi) is recalling one 2019 Audi Q3 vehicle. Production deviation in the belt pully can prevent the circlip from properly engaging the steering rack.
critical fastenersVolkswagen Group of America, Inc.
VehicleJan 26, 2021
Subaru of shift linkage/cable/rod recall — NHTSA campaign 21V024000
Subaru of America, Inc. (Subaru) is recalling certain 2021 Outback and Impreza vehicles. The continuously variable transmission (CVT) select lever cable nut may not have been tightened…
shift linkage/cable/rodSubaru of America, Inc.
Medical DeviceJan 20, 2021
Fresenius Medical Care Holdings NaturaLyte Liquid Acid concentrate bottles, Model Number recall — FDA Z-0815-2021
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
Medical DeviceJan 20, 2021
Fresenius Medical Care Holdings NaturaLyte Liquid Acid concentrate drums, Model Number recall — FDA Z-0826-2021
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
Medical DeviceJan 20, 2021
Boston Scientific Lotus Edge Valve System, Transcatheter Aortic Valve Prosthesis Premounted recall — FDA Z-0734-2021
Failure to execute the visual inspection correctly prior to locking the valve during the deployment process can lead to the inability to release the delivery system.
Class IFDA: TerminatedBoston Scientific Corporation
Medical DeviceJan 20, 2021
Fresenius Medical Care Holdings Citrasate Liquid Acid concentrate drums, Model Number recall — FDA Z-0828-2021
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
Medical DeviceJan 20, 2021
Clerio Vision, extreme H2O monthly, MED, DIA 14.0 PWR -2.25, UPC 675506803334 (6 count) and recall — FDA Z-0808-2021
One lot of contact lenses labeled as BC MED, DIA 14.0 PWR -2.25 contained BC MED, DIA 14.0, PWR -3.75 contact lenses
Class IIFDA: TerminatedClerio Vision
Medical DeviceJan 20, 2021
Fresenius Medical Care Holdings Naturalyte Liquid Acid concentrate bottles, Product Code recall — FDA Z-0835-2021
The deviation in conductivity for sodium level exceeds 0.6mS/cm from the theoretical conductivity (TCD) or approximately 6mEq/L of sodium from prescriptions that was previously…
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
Medical DeviceJan 20, 2021
Fresenius Medical Care Holdings Citrasate Liquid Acid concentrate drums, Model Number recall — FDA Z-0829-2021
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
Medical DeviceJan 20, 2021
Fresenius Medical Care Holdings Naturalyte Liquid Acid concentrate drums, Product Code recall — FDA Z-0840-2021
The deviation in conductivity for sodium level exceeds 0.6mS/cm from the theoretical conductivity (TCD) or approximately 6mEq/L of sodium from prescriptions that was previously…
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.