FoodMar 15, 2023
Titans Global JSJ DMC Leaf Cake 3.35 oz recall — FDA F-0412-2023
Product was found to have the presence of egg, which is not declared on the label.
Class IFDA: TerminatedTitans Global Inc.
March 2023 recalls — page 25
These records include useful source details for the selected month.
FoodMar 15, 2023
Chukar Cherry Company item #21508, net wt recall — FDA F-0417-2023
undeclared hazelnuts
Class IFDA: TerminatedChukar Cherry Company Inc.
DrugMar 15, 2023
Amerisource Health Services Verapamil Hydrochloride Extended-Release Tablets, USP, 120 mg recall — FDA D-0436-2023
Failed Dissolution Specification: Out of specification dissolution results at time point zero. The OOS was above specified values.
Class IIFDA: TerminatedAmerisource Health Services LLC
DrugMar 15, 2023
Nutraceutical NaturalCare, children's, Allergy Care, Homeopathic, 4 Months and Up, Liquid recall — FDA D-0440-2023
CGMP Deviations: Raw material recalled by repackager, due to discoloration.
Class IIFDA: OngoingNutraceutical Corporation
DrugMar 15, 2023
Teva Pharmaceuticals USA Metformin hydrochloride Extended-Release Tablets, 1000 mg, 60-count recall — FDA D-0441-2023
CGMP Deviations: Detection of N-Nitrosodimethylamine (NDMA) levels in excess of the Acceptable Daily Intake Limit.
Class IIFDA: TerminatedTeva Pharmaceuticals USA Inc.
DrugMar 15, 2023
Nutraceutical NatraBio, Cold& Sinus Nasal Spray, Homeopathic Medicine, 0.8 FL Oz. ( 24ml) recall — FDA D-0438-2023
CGMP Deviations: Raw material recalled by repackager, due to discoloration.
Class IIFDA: OngoingNutraceutical Corporation
DrugMar 15, 2023
Pharmedica USA Purely Soothing 15% MSM Drops recall — FDA D-0456-2023
Non-Sterility
Class IFDA: OngoingPharmedica USA, LLC
DrugMar 15, 2023
Brimonidine Tartrate Ophthalmic Solution 0.15% recall — FDA D-0433-2023
Lack of sterility assurance: Cracks have developed in some of the units caps of Brimonidine tartrate ophthalmic solution bottles. There is a possibility the broken cap may impact sterility.
Class IIFDA: CompletedApotex Corp.
DrugMar 15, 2023
Nanomaterials Discovery Snowy Range Blue Alcohol Antiseptic 80% Topical Solution Hand recall — FDA D-0455-2023
Chemical Contamination: FDA analysis found the product to contain methanol, acetaldehyde, and acetal above the limits.
Class IFDA: OngoingNanomaterials Discovery Corporation
VehicleMar 10, 2023
Maverick tail lights recall — NHTSA campaign 23V160000
Ford Motor Company (Ford) is recalling certain 2023 Maverick vehicles. A missing electrical circuit may cause the trailer taillights to not illuminate as intended when utilizing the vehicle…
tail lightsFord Motor Company
VehicleMar 10, 2023
Bronco camera recall — NHTSA campaign 23V165000
Ford Motor Company (Ford) is recalling certain 2021-2022 Bronco vehicles equipped with 8-inch SYNC infotainment screens that were previously remedied under recall 22V-825. The rearview…
cameraFord Motor Company
VehicleMar 10, 2023
F-150 linkages recall — NHTSA campaign 23V163000
Ford Motor Company (Ford) is recalling certain 2021 F-150 vehicles. The windshield wiper arms may break, causing the windshield wipers to fail.
linkagesFord Motor Company
VehicleMar 9, 2023
Honda buckle recall — NHTSA campaign 23V158000
Honda (American Honda Motor Co.) is recalling certain 2017-2020 CR-V, 2018-2019 Accord and Accord Hybrid, 2018-2020 Odyssey, 2019 Insight, and 2019-2020 Acura RDX vehicles. A manufacturing…
buckleHonda (American Honda Motor Co.)
Medical DeviceMar 8, 2023
Covidien Surgipro Monofilament Polypropylene Sutures Product Description CP-535 SURGIPRO* 1 recall — FDA Z-1179-2023
Sterile Barrier Breach of Breather Pouch may cause infection or vision loss for ophthalmic procedures in cases where there is direct patient contact
Class IIFDA: OngoingCovidien, LP
Medical DeviceMar 8, 2023
Beaver Visitec International CustomEyes kits recall — FDA Z-1200-2023
Device packaging may contain open seals, compromising product sterility.
Class IIFDA: OngoingBeaver Visitec International, Inc.
Medical DeviceMar 8, 2023
Unetixs Vascular MultiLab Series II LHS TI & ERGO non-invasive vascular diagnostic device recall — FDA Z-1194-2023
The current luer fittings and adaptors allow for the possibility of the air line to be misconnected to an intravenous line, which may cause an air embolism.
Class IIFDA: OngoingUnetixs Vascular, Inc.
Medical DeviceMar 8, 2023
Covidien Novafil Monofilament Polybutester Suture Product Description: 8886 4002-41 NOVAFIL recall — FDA Z-1175-2023
Sterile Barrier Breach of Breather Pouch may cause infection or vision loss for ophthalmic procedures in cases where there is direct patient contact
Class IIFDA: OngoingCovidien, LP
Medical DeviceMar 8, 2023
Wright Medical Technology ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 402S0425, Bone recall — FDA Z-1169-2023
Stryker has identified an issue that impacts two specific lots of CLAW" II plates. The plates within these two lots were found to have been comingled, resulting in the incorrect product in…
Class IIFDA: OngoingWright Medical Technology, Inc.
Medical DeviceMar 8, 2023
Unetixs Vascular MultiLab Series II REVO non-invasive vascular diagnostic device, Model recall — FDA Z-1196-2023
The current luer fittings and adaptors allow for the possibility of the air line to be misconnected to an intravenous line, which may cause an air embolism.
Class IIFDA: OngoingUnetixs Vascular, Inc.
Medical DeviceMar 8, 2023
stryker Hoffmann LRF, Transport Strut, Model Number 4933-0-400 recall — FDA Z-1191-2023
Stryker has identified a nonconformance in specific lots of Hoffmann LRF Bone Transport Struts. Specifically, the thread pitch is oversized at the distal end of the threaded rod, and as a…
Class IIFDA: OngoingStryker GmbH
Medical DeviceMar 8, 2023
Stryker Finished Goods Box of 50 Inserts and Scanning Labels for Medivac Guardian 2L recall — FDA Z-1184-2023
Triton Canister Software, Insert & Scanning Label may cause the Triton Canister System to output inaccurate blood loss estimates can lead to confusion and could potentially result in either…
Class IIFDA: OngoingStryker Corporation
Medical DeviceMar 8, 2023
Covidien Monofilament Nylon Suture (McKesson Branded) and Coated Braided Silk Suture recall — FDA Z-1173-2023
Sterile Barrier Breach of Breather Pouch may cause infection or vision loss for ophthalmic procedures in cases where there is direct patient contact
Class IIFDA: OngoingCovidien, LP
Medical DeviceMar 8, 2023
Encore Medical EMPOWR VVC KNEE TIBIAL INSERT, SIZE 6, 22MM, REF: 346-22-706 recall — FDA Z-1187-2023
Tibial insert implant large boxes were labeled small and the small boxes were labeled large. If the incorrect labeling is identified this could lead to surgical delay and if the surgeon…
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceMar 8, 2023
Baxter Healthcare Life2000 Ventilator PKG, Hospital, a) REF BT20007, b) REF BT-20-0007 recall — FDA Z-1140-2023
There is the potential for patient desaturation events to occur under certain scenarios when the Life2000 ventilation system is connected with an oxygen concentrator.
Class IFDA: OngoingBaxter Healthcare Corporation
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.