FoodJul 19, 2023
International Food Companies DBA International 1st phorm Level-1 Sustained Assimilation recall — FDA F-1247-2023
Product may contain Staphylococcus aureus.
Class IIFDA: TerminatedInternational Food Companies DBA International Food…
July 2023 recalls — page 7
These records include useful source details for the selected month.
FoodJul 19, 2023
Dakota Style 1 recall — FDA F-1243-2023
May contain undeclared milk
Class IFDA: TerminatedDakota Style, Inc.
FoodJul 19, 2023
Dakota Style 1 recall — FDA F-1241-2023
May contain undeclared milk
Class IFDA: TerminatedDakota Style, Inc.
FoodJul 19, 2023
International Food Companies DBA International 1st phorm Level-1 Sustained Assimilation recall — FDA F-1246-2023
Product may contain Staphylococcus aureus.
Class IIFDA: TerminatedInternational Food Companies DBA International Food…
FoodJul 19, 2023
Oregon Potato Company Great Value Sliced Strawberries recall — FDA F-1232-2023
Potential contamination with Hepatitis A.
Class IFDA: TerminatedOregon Potato Company
FoodJul 19, 2023
Garelick Farms Tampico brand Mango Punch recall — FDA F-1245-2023
Product contains undeclared Yellow 5.
Class IIFDA: TerminatedGarelick Farms LLC
FoodJul 19, 2023
Oregon Potato Company Rader Farms Organic Fresh Start Smoothie Blueberry recall — FDA F-1236-2023
Potential contamination with Hepatitis A.
Class IFDA: TerminatedOregon Potato Company
FoodJul 19, 2023
Wawona Frozen Foods 4 lb. plastic bags - 10 bags per case Keep Frozen Item# 684779 UPC: 0 recall — FDA F-1231-2023
Product may contain Hepatitis A
Class IFDA: TerminatedWawona Frozen Foods Inc.
DrugJul 19, 2023
Tenn South Distillery LLC dba Big Machine Big Machine Distillery Hand Sanitizer Non-Sterile recall — FDA D-0915-2023
CGMP Deviation: impurities exceed allowable limits.
Class IIFDA: OngoingTenn South Distillery LLC dba Big Machine Distillery
DrugJul 19, 2023
SUNMARK EYE DROPS ORIGINAL FORMULA Original Eye Drops recall — FDA D-0897-2023
CGMP Deviations: good manufacturing deficiencies related to a lack of documentation of the fill line.
Class IIFDA: OngoingK.C. Pharmaceuticals, Inc.
DrugJul 19, 2023
Global Pharma Healthcare Private Delsam Pharma's ARTIFICIAL TEARS recall — FDA D-0922-2023
CGMP Deviations: All other lots of eye drops are being recalled due to CGMP Deviations because they were manufactured in the same facility under the same conditions as the lots found to be…
Class IIFDA: OngoingGlobal Pharma Healthcare Private Limited
DrugJul 19, 2023
Atropine Sulfate Injection, USP 8 mg per 20 mL (0.4 mg per mL), 20 mL Multiple Dose Vials recall — FDA D-0917-2023
Presence of Particulate Matter: Particulate matter identified as fiber.
Class IIFDA: TerminatedAccord Healthcare, Inc.
DrugJul 19, 2023
Global Pharma Healthcare Private Artificial Tears recall — FDA D-0920-2023
CGMP Deviations: All other lots of eye drops are being recalled due to CGMP Deviations because they were manufactured in the same facility under the same conditions as the lots found to be…
Class IIFDA: OngoingGlobal Pharma Healthcare Private Limited
DrugJul 19, 2023
Albuterol Sulfate Inhalation Aerosol, 90 mcg, 200 Metered Inhalation, net content 6.7 g recall — FDA D-0938-2023
Defective container: empty inhaler and leakage observed through the inhaler valve due to partially missing bottom seat (gasket).
Class IFDA: TerminatedCipla USA, Inc.
DrugJul 19, 2023
Global Pharma Healthcare Private Delsam Pharma's ARTIFICIAL TEARS recall — FDA D-0921-2023
Non-Sterility: FDA analysis found unopened products to have bacterial contamination.
Class IFDA: OngoingGlobal Pharma Healthcare Private Limited
DrugJul 19, 2023
Bivalirudin for Injection 250 mg, 10 Single-Dose Vials recall — FDA D-0918-2023
Presence of Particulate Matter: Particulate matter identified as fiber.
Class IIFDA: TerminatedAccord Healthcare, Inc.
DrugJul 19, 2023
Amlodipine Besylate Tablets, USP 10 mg, 1000-count bottles recall — FDA D-0899-2023
Subpotent Drug: Out-of-Specification test results observed in assay test at 21-month long term stability study.
Class IIIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugJul 19, 2023
Global Pharma Healthcare Private Artificial Tears recall — FDA D-0919-2023
Non-Sterility: FDA analysis found unopened products to have bacterial contamination.
Class IFDA: OngoingGlobal Pharma Healthcare Private Limited
DrugJul 19, 2023
Tiagabine Hydrochloride Tablets, 2 mg, 30-count bottle recall — FDA D-0914-2023
Failed Impurities: Out of Specification (OOS) result observed during Related Substances testing
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJul 19, 2023
Sunitinib Malate Capsules, 12.5 mg, 28-count bottles recall — FDA D-0913-2023
Failed Moisture Limits: Water (moisture) content above the approved product specifications.
Class IIFDA: TerminatedTeva Pharmaceuticals USA Inc.
DrugJul 19, 2023
EQUATE EYE DROPS DRY EYE RELIEF Dry Eye Relief Lubricant Eye Drops recall — FDA D-0898-2023
CGMP Deviations: good manufacturing deficiencies related to a lack of documentation of the fill line.
Class IIFDA: OngoingK.C. Pharmaceuticals, Inc.
VehicleJul 14, 2023
Tesla front recall — NHTSA campaign 23V488000
Tesla, Inc. (Tesla) is recalling certain 2021-2023 Model S and Model X vehicles. The front-row seat belts may not be connected properly to the pretensioner anchors, which can cause the seat…
frontTesla, Inc.
VehicleJul 14, 2023
Tesla camera recall — NHTSA campaign 23V489000
Tesla, Inc. (Tesla) is recalling certain 2023 Model S, Model X, and Model Y vehicles. The forward-facing camera may be misaligned, causing some of the active safety features such as…
cameraTesla, Inc.
Medical DeviceJul 12, 2023
Waldemar Link GmbH & Co. KG LinkSymphoKnee Distal Femoral Augment - Tilastan - Size 7-8 recall — FDA Z-2066-2023
Fixation screw was inserted through the wrong side of the augment (distal to proximal, as opposed to proximal to distal, which is the correct orientation).
Class IIFDA: OngoingWaldemar Link GmbH & Co. KG (Mfg Site)
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.