DrugSep 21, 2022
Vi-Jon meijer, magnesium citrate Saline Laxative, Oral Solution, (1.745 g/fl oz), Lemon recall — FDA D-1504-2022
Microbial contamination of non-sterile products.
Class IFDA: TerminatedVi-Jon, LLC
Monthly breakdown
2022 recalls by month
Select a month to review the recall records reported during that period.
December 2022318 records · 4 categoriesNovember 2022270 records · 4 categoriesOctober 2022288 records · 4 categoriesSeptember 2022318 records · 4 categoriesAugust 2022293 records · 4 categoriesJuly 2022334 records · 4 categoriesJune 2022348 records · 4 categoriesMay 2022227 records · 4 categoriesApril 2022205 records · 4 categoriesMarch 2022449 records · 4 categoriesFebruary 2022237 records · 4 categoriesJanuary 2022296 records · 4 categories
2022 recalls — page 43
Records are ordered by the best available source date.
DrugSep 21, 2022
Vi-Jon Magnesium Citrate SALINE LAXATIVE, Oral Solution, 1.745 g, Grape Flavor, 10 FL OZ recall — FDA D-1513-2022
CGMP Deviations;
Class IIFDA: TerminatedVi-Jon, LLC
DrugSep 21, 2022
CITROMA Magnesium Citrate SALINE LAXATIVE, Oral Solution, 1.745 g, Lemon Flavor, 10 FL OZ recall — FDA D-1511-2022
CGMP Deviations
Class IIFDA: TerminatedVi-Jon, LLC
DrugSep 21, 2022
MAGNESIUM CITRATE P, magnesium citrate SALINE LAXATIVE, Oral Solution, (1.745 g/fl oz) recall — FDA D-1505-2022
Microbial contamination of non-sterile products.
Class IFDA: TerminatedVi-Jon, LLC
DrugSep 21, 2022
Pine Pharmaceuticals Bupivacaine HCl 0.375% w/v and Lidocaine HCl 2% w/v Solution for recall — FDA D-1514-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedPine Pharmaceuticals, LLC
DrugSep 21, 2022
MAGNESIUM CITRATE Kroger, Magnesium Citrate SALINE LAXATIVE, Oral Solution, 1.745 g, Lemon recall — FDA D-1503-2022
Microbial contamination of non-sterile products.
Class IFDA: TerminatedVi-Jon, LLC
DrugSep 21, 2022
PROPOFOL Injectable Emulsion, 1 g/100 mL (10 mg/mL) recall — FDA D-1540-2022
Presence of particulate matter
Class IFDA: TerminatedPfizer Inc.
DrugSep 21, 2022
RemedyRepack Lisinopril 10 mg tablets, 30-count Blister Card recall — FDA D-1538-2022
Presence of Foreign Substance: Foreign material (metal piece) embedded in one tablet.
Class IIFDA: TerminatedRemedyRepack Inc.
DrugSep 21, 2022
Vi-Jon Walgreens, Dye-Free, Magnesium Citrate, SALINE LAXATIVE, Oral Solution recall — FDA D-1509-2022
Microbial contamination of non-sterile products.
Class IFDA: TerminatedVi-Jon, LLC
DrugSep 21, 2022
Lisinopril Tablets USP, 10 mg, 1000-count bottles recall — FDA D-1536-2022
Presence of Foreign Substance: Foreign material (metal piece) embedded in one tablet.
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
VehicleSep 19, 2022
Audi Q3 glass, side/rear recall — NHTSA campaign 22V701000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2022 Audi Q3 vehicles. A window manufacturing error may allow the rear window to crack or break.
glass, side/rearVolkswagen Group of America, Inc.
VehicleSep 19, 2022
Tesla power window devices and controls recall — NHTSA campaign 22V702000
Tesla, Inc. (Tesla) is recalling certain 2017-2022 Model 3, 2020-2022 Model Y, and 2021-2022 Model S and Model X vehicles. The window automatic reversal system may not react correctly after…
power window devices and controlsTesla, Inc.
VehicleSep 19, 2022
Kia trailer hitch recall — NHTSA campaign 22V703000
Kia America, Inc. (Kia) is recalling certain 2016-2022 Sorento, 2021-2022 Sorento Hybrid (HEV), 2022-2023 Sorento Plug-In Hybrid (PHEV), and 2017-2022 Sportage vehicles equipped with a tow…
trailer hitchKia America, Inc.
Medical DeviceSep 14, 2022
American Contract Systems Various PICC Line, Central Line Packs recall — FDA Z-1692-2022
Product was exposed to multiple sterilization cycles without validation for multiple exposures.
Class IIFDA: OngoingAmerican Contract Systems, Inc.
Medical DeviceSep 14, 2022
Philips OmniLab Advanced+, Rx Only recall — FDA Z-1657-2022
Motor assemblies manufactured with nonconforming plastic that contributes to off-gassing of VOCs.
Class IFDA: OngoingPhilips Respironics, Inc.
Medical DeviceSep 14, 2022
Biosense Webster CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath, REF: D138501 recall — FDA Z-1677-2022
Outside packaging for a device indicated for introducing cardiovascular catheters into the heart, sustained water damage, which may have affected the sterile barrier of the product inside.…
Class IIFDA: OngoingBiosense Webster, Inc.
Medical DeviceSep 14, 2022
Abbott Alinity m SARS-CoV-2 CTRL Kit, REF 09N78-085, each kit contains 12 x 1.3mL CTRL - and recall — FDA Z-1679-2022
Reports received of an increase of message code 9186 (internal control failed) when using the kit.
Class IIFDA: OngoingAbbott Molecular, Inc.
Medical DeviceSep 14, 2022
Philips BiPAP A40, Rx Only recall — FDA Z-1655-2022
Motor assemblies manufactured with nonconforming plastic that contributes to off-gassing of VOCs.
Class IFDA: OngoingPhilips Respironics, Inc.
Medical DeviceSep 14, 2022
Datascope Insertion Kit for use with SENSATION PLUS 8F. 50cc Intra-Aortic Balloon Catheter recall — FDA Z-1687-2022
Certain lots containing undersized dilator.
Class IIFDA: OngoingDatascope Corporation
Medical DeviceSep 14, 2022
Ortho-Clinical Diagnostics VITROS XT 3400 Chemistry System with Version 3.7.2 and below recall — FDA Z-1675-2022
Performing a system shutdown on VITROS XT 3400 and VITROS XT 7600 Systems may cause a positive or negative shift in the electrical current supplied to the LED used in conjunction with the…
Class IIFDA: OngoingOrtho-Clinical Diagnostics, Inc.
Medical DeviceSep 14, 2022
OrthoPediatrics Orthex External Fixation Wire Sharp Bayonet 1.8 x 400 mm Model: K400-18BN recall — FDA Z-1678-2022
Manufacturing variance near transition of tip is increasing the likelihood the wire tip may fracture. The fractured tip may be retained in the patient. Retrieval attempts may be made which…
Class IIFDA: OngoingOrthoPediatrics Corp
Medical DeviceSep 14, 2022
Philips OmniLab Advanced + with Heated Tube Humidifier, Rx Only recall — FDA Z-1659-2022
Motor assemblies manufactured with nonconforming plastic that contributes to off-gassing of VOCs.
Class IFDA: OngoingPhilips Respironics, Inc.
Medical DeviceSep 14, 2022
American Contract Systems Various Pacemaker Packs, Cardio Thoracic Packs recall — FDA Z-1691-2022
Product was exposed to multiple sterilization cycles without validation for multiple exposures.
Class IIFDA: OngoingAmerican Contract Systems, Inc.
Medical DeviceSep 14, 2022
Philips OmniLab Advanced+ Intl (Flow Gen), Rx Only recall — FDA Z-1658-2022
Motor assemblies manufactured with nonconforming plastic that contributes to off-gassing of VOCs.
Class IFDA: OngoingPhilips Respironics, Inc.
About the 2022 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.