FoodMar 23, 2022
The Royal Ice Cream Company All Ice Cream and Ice Cream products within expiry recall — FDA F-0863-2022
Product may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedThe Royal Ice Cream Company Inc.
Latest records
Latest recalls — page 753
The newest recall records with useful source details are listed here.
FoodMar 23, 2022
RMJV, LP dba Fresh Creative Foods Fresh Creative Foods THAI NOODLE SALAD NO CORN BULK 2/5 LB recall — FDA F-0890-2022
During manufacturing pieces of hard clear plastic was found. Upon investigation the source was identified as ice purchased from supplier.
Class IIFDA: TerminatedRMJV, LP dba Fresh Creative Foods
FoodMar 23, 2022
RMJV, LP dba Fresh Creative Foods Fresh Creative Foods AUTUMN COUSCOUS W/ BUTTERNUT SQUASH recall — FDA F-0894-2022
During manufacturing pieces of hard clear plastic was found. Upon investigation the source was identified as ice purchased from supplier.
Class IIFDA: TerminatedRMJV, LP dba Fresh Creative Foods
FoodMar 23, 2022
Candies Tolteca Tolteca Saladitos Salted Dried Plums recall — FDA F-0857-2022
Firm distributed Dried Salted Plum (Saladitos) that may contain high lead levels.
Class IIFDA: TerminatedCandies Tolteca
FoodMar 23, 2022
RMJV, LP dba Fresh Creative Foods Fresh Creative Foods THAI PEANUT DRESSING R&G 80/2.5 OZ recall — FDA F-0887-2022
During manufacturing pieces of hard clear plastic was found. Upon investigation the source was identified as ice purchased from supplier.
Class IIFDA: TerminatedRMJV, LP dba Fresh Creative Foods
FoodMar 23, 2022
Gourmet Kitchen 14" Raw Buttermilk Breakfast Tart with Fresh Blueberries & recall — FDA F-0866-2022
Undeclared almonds
Class IFDA: TerminatedGourmet Kitchen, Inc.
FoodMar 23, 2022
Candies Tolteca Tolteca Saladitos con Chile Limon, Dried Plums with Chili & recall — FDA F-0858-2022
Firm distributed Dried Salted Plum (Saladitos) that may contain high lead levels.
Class IIFDA: TerminatedCandies Tolteca
FoodMar 23, 2022
RMJV, LP dba Fresh Creative Foods Fresh Creative Foods LEMON CAPELLINI SALAD 2/4.5 LB recall — FDA F-0888-2022
During manufacturing pieces of hard clear plastic was found. Upon investigation the source was identified as ice purchased from supplier.
Class IIFDA: TerminatedRMJV, LP dba Fresh Creative Foods
FoodMar 23, 2022
Swanson Ultra: Vitamin B12 Methylcobalamin High Absorption 60 recall — FDA F-0867-2022
Dietary supplement may contain potential metal shavings greater than or equal to 7mm in length.
Class IIFDA: TerminatedSwanson Health Products, Inc.
FoodMar 23, 2022
RMJV, LP dba Fresh Creative Foods Freshness Guaranteed BROCCOLI CHEDDAR PASTA SALAD WM 6/14 recall — FDA F-0891-2022
During manufacturing pieces of hard clear plastic was found. Upon investigation the source was identified as ice purchased from supplier.
Class IIFDA: TerminatedRMJV, LP dba Fresh Creative Foods
FoodMar 23, 2022
RMJV, LP dba Fresh Creative Foods Fresh Creative Foods recall — FDA F-0893-2022
During manufacturing pieces of hard clear plastic was found. Upon investigation the source was identified as ice purchased from supplier.
Class IIFDA: TerminatedRMJV, LP dba Fresh Creative Foods
DrugMar 23, 2022
The Harvard Drug Group hydrALAZINE HCl Tablets, USP, 10 mg, 100 Tablets per carton recall — FDA D-0653-2022
Failed Impurities/Degradation Specifications: Out of specification result obtained during routine stability testing for Impurities.
Class IIFDA: TerminatedThe Harvard Drug Group
DrugMar 23, 2022
Walmart Stores Avaphinal Maximum Male Enhancement Sexual Pills, 2000 MG* recall — FDA D-0725-2022
Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared sildenafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making…
Class IFDA: TerminatedWalmart Stores
VehicleMar 23, 2022
Volkswagen Group of suspension recall — NHTSA campaign 22V176000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2022 Tiguan, Taos, and 2021 Tiguan long wheel base (LWB) vehicles. A second notice will be sent once remedy parts become…
suspensionVolkswagen Group of America, Inc.
VehicleMar 18, 2022
Tesla display function recall — NHTSA campaign 22V169000
Tesla, Inc. (Tesla) is recalling certain 2018-2019 Model S, Model X, and 2017-2020 Model 3 vehicles equipped with Autopilot Computer 2.5 and operating certain firmware releases. The…
display functionTesla, Inc.
Medical DeviceMar 16, 2022
Lusys Laboratories COVID-19 IgG/IGM Antibody Test For Detection of COVID-19 IgG and IgM recall — FDA Z-0718-2022
COVID-19 test kits (Antibody Rapid Test kit and Antigen Rapid Test Kit) are not authorized, cleared, or approved for marketing and/or distribution in the U.S.
Class IFDA: OngoingLusys Laboratories, Inc.
Medical DeviceMar 16, 2022
Maquet Cardiovascular HEMASHIELD GOLD KNITTED MICROVEL DOUBLE VELOUR VASCULAR GRAFT- D: 7 mm recall — FDA Z-0729-2022
Outer labelling (HEMASHIELD GOLD Knitted Microvel Double Velour Bifurcated Vascular Graft, D: 16 x 8 mm; L: 40 cm) does not correspond to the (inner) sterile packaging labelling (HEMASHIELD…
Class IIFDA: TerminatedMaquet Cardiovascular, LLC
Medical DeviceMar 16, 2022
LuSys 2nd Generation of COVID-19 Viral Antigen Test For all mutant variety Cat: I-114 recall — FDA Z-0716-2022
COVID-19 test kits (Antibody Rapid Test kit and Antigen Rapid Test Kit) are not authorized, cleared, or approved for marketing and/or distribution in the U.S.
Class IFDA: OngoingLusys Laboratories, Inc.
Medical DeviceMar 16, 2022
Nextremity Solutions Nextra Cannulated Hammertoe Standard Instrument Kit-indicated for small recall — FDA Z-0740-2022
During insertion of the middle phalanx implant into bone, the driver may deform the implant locking mechanism and result in inadequate mating force between the middle and proximal phalanx…
Class IIFDA: TerminatedNextremity Solutions
Medical DeviceMar 16, 2022
Medtronic Xomed NIM TRIVANTAGE EMG Endotracheal Tube recall — FDA Z-0743-2022
There is potential for multiple issues due to a manufacturing nonconformity.
Class IIFDA: OngoingMedtronic Xomed, Inc.
Medical DeviceMar 16, 2022
Ion Beam Applications S.A ProteusPLUS and ProteusONE- designed to produce and deliver a recall — FDA Z-0747-2022
When resuming from a beam pause, the Proton Therapy System does not verify whether the beam range has not been manually modified during the pause and is still the prescribed one. Therefore,…
Class IIFDA: OngoingIon Beam Applications S.A.
Medical DeviceMar 16, 2022
Carl Zeiss Meditec CIRRUS HD-OCT, Models 5000 AngioPlex and 6000 AngioPlex recall — FDA Z-0723-2022
Optic nerve head angiography scan to be turned off due to its distribution without pre-market clearance.
Class IIFDA: OngoingCarl Zeiss Meditec, Inc.
Medical DeviceMar 16, 2022
RAYSEARCH LABORATORIES AB RayStation/RayPlan- designed for treatment planning and analysis recall — FDA Z-0732-2022
If a new primary image set is selected while the cine loop is running, the primary image set will be displayed as both primary and secondary image set in all side-by-side views. This will…
Class IIFDA: OngoingRAYSEARCH LABORATORIES AB
Medical DeviceMar 16, 2022
Nextremity Solutions Nextra CH Cannulated Hammertoe Mini Instrument Kit-indicated for small recall — FDA Z-0739-2022
During insertion of the middle phalanx implant into bone, the driver may deform the implant locking mechanism and result in inadequate mating force between the middle and proximal phalanx…
Class IIFDA: TerminatedNextremity Solutions
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026110 records · 3 categoriesSeptember 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories