DrugAug 14, 2024
Sevelamer Carbonate for Oral Suspension 0.8g packets recall — FDA D-0625-2024
Labeling: Incorrect or Missing Lot and/or Exp Date. Missing lot number and expiration dates on packets
Class IIIFDA: OngoingDr. Reddy's Laboratories, Inc.
Latest records
Latest recalls — page 362
The newest recall records with useful source details are listed here.
DrugAug 14, 2024
Amneal Pharmaceuticals Methotrexate Tablets, USP, 2.5mg, 100-count Bottle recall — FDA D-0629-2024
Presence of Foreign Tablets: Potential presence of Fludrocortisone Acetate Tablet USP 0.1 mg within the Methotrexate 2.5 mg 100-count Bottle.
Class IIIFDA: CompletedAmneal Pharmaceuticals, LLC
DrugAug 14, 2024
Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles recall — FDA D-0631-2024
Labeling: Label Mix-Up: Some bottles of Acetaminophen Extra Strength 500 mg tablets were incorrectly labeled with the drug facts label for Aspirin 81 mg tablets.
Class IFDA: TerminatedA-S Medication Solutions LLC
DrugAug 14, 2024
Empower Pharmacy, Estradiol Cypionate Injection, 10mg/mL, 5mL Sterile Multiple Dose Vial recall — FDA D-0630-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedEMPOWER CLINIC SERVICES LLC
DrugAug 14, 2024
PEG-3350, Sodium Sulfate, Sodium Chloride, Potassium Chloride, Sodium Ascorbate, and recall — FDA D-0628-2024
Defective container: potential for non-sealed pouches which can lead to product leakage.
Class IIIFDA: TerminatedNovel Laboratories, Inc. d.b.a Lupin Somerset
DrugAug 14, 2024
Granules Consumer Health Acetaminophen, USP 500mg, Pain Reliever/Fever Reducer, Extra recall — FDA D-0627-2024
Label mix-up: Carton incorrectly labeled.
Class IIIFDA: TerminatedGranules Consumer Health Inc.
VehicleAug 10, 2024
Explorer engine recall — NHTSA campaign 24V598000
Ford Motor Company (Ford) is recalling certain 2020-2022 Explorer vehicles equipped with the Police Interceptor Utility Package. In the event of an engine failure, engine oil and fuel vapor…
engineFord Motor Company
VehicleAug 9, 2024
Maverick body control module/bcm recall — NHTSA campaign 24V590000
Ford Motor Company (Ford) is recalling certain 2022 Maverick vehicles previously repaired under recall number 24V-267. The body and power train control modules may fail to detect a change…
body control module/bcmFord Motor Company
VehicleAug 9, 2024
Ford motor recall — NHTSA campaign 24V594000
Ford Motor Company (Ford) is recalling certain 2023-2024 Maverick, Ford Bronco Sport, and Mustang Mach-E vehicles. The front windshield wiper motor may become inoperative, causing the…
motorFord Motor Company
VehicleAug 9, 2024
Mustang rear recall — NHTSA campaign 24V593000
Ford Motor Company (Ford) is recalling certain 2024 Mustang vehicles. The rear suspension knuckles may have a casting defect that causes them to fail, which can result in a loss of vehicle…
rearFord Motor Company
VehicleAug 8, 2024
Jeep Wrangler tail lights recall — NHTSA campaign 24V585000
Chrysler (FCA US, LLC) is recalling certain 2024 Jeep Wrangler vehicles. The vehicles are equipped with incorrect tail lights that may be obstructed by the spare tire. As such, these…
tail lightsChrysler (FCA US, LLC)
Medical DeviceAug 7, 2024
Boston Scientific Capio SLIM Suture Capturing Device, 1-Pack, UPN: M0068318250 recall — FDA Z-2452-2024
Some lots of Capio SLIM do not consistently catch the suture after activation possibly resulting in a prolonged procedure or additional medical intervention.
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceAug 7, 2024
Angiodynamics SOFT-VU KUMPE 5F X 65CM -Used for patients in need of angiographic diagnosis recall — FDA Z-2454-2024
Mislabeled. The shelf-box labeling (unit of sale) is accurate for the packaged devices, however the inner pouch label may contain information for a different model (catheter length)
Class IIFDA: OngoingAngiodynamics, Inc.
Medical DeviceAug 7, 2024
Zimmer CPT Hip Joint Metal/Polymer Semi-Constrained Cemented Prosthesis, used in Hip recall — FDA Z-2450-2024
Affected product has an increased risk of postoperative perisprosthetic femoral fracture (PFF). The IFU is being updated to reflect the risk of PFF.
Class IIFDA: OngoingZimmer, Inc.
Medical DeviceAug 7, 2024
Becton Dickinson Infusion Therapy Systems BD Insyte Autoguard BC, Shielded IV Catheter with recall — FDA Z-2458-2024
Catheters may contain a hole in the catheter tubing, which could result in leakage during the insertion process.
Class IIFDA: OngoingBecton Dickinson Infusion Therapy Systems, Inc.
Medical DeviceAug 7, 2024
Boston Scientific Capio SLIM Suture Capturing Device, Box of 5, Outer Package UPN recall — FDA Z-2451-2024
Some lots of Capio SLIM do not consistently catch the suture after activation possibly resulting in a prolonged procedure or additional medical intervention.
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceAug 7, 2024
BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, for FILMARRAY recall — FDA Z-2456-2024
If blood culture identification panel is used in conjunction with specific lots of culture media bottles, then false positive Serratia marcescens results may occur, due to an increased…
Class IIFDA: OngoingBioFire Diagnostics, LLC
Medical DeviceAug 7, 2024
Medivance Arctic Sun Temperature Management Systems, Name/REF: Arctic Sun STAT recall — FDA Z-2457-2024
If temperature management system fails to reach correct target water temperature while device is operating in patient control mode, due to sudden patient temperature changes/interruption in…
Class IIFDA: OngoingMedivance Inc.
Medical DeviceAug 7, 2024
EVIDENT SCIENTIFIC SlideView VS200 slide viewer recall — FDA Z-2416-2024
A broken fuse inside the laser that was caused by a short circuit at PIN 4 of the DOOR CTRL. This short circuit was caused by a badly positioned cable that made contact with the…
Class IIFDA: OngoingEVIDENT SCIENTIFIC Inc.
Medical DeviceAug 7, 2024
Angiodynamics SOFT-VU KUMPE 5F X 40CM -Used for patients in need of angiographic diagnosis recall — FDA Z-2453-2024
Mislabeled. The shelf-box labeling (unit of sale) is accurate for the packaged devices, however the inner pouch label may contain information for a different model (catheter length)
Class IIFDA: OngoingAngiodynamics, Inc.
Medical DeviceAug 7, 2024
Beckman Coulter Mishima K.K DxC 500 AU Clinical Chemistry Analyzer, REF C63520 is an recall — FDA Z-2455-2024
There are two software bug issues with the analyzer. Issue 1: When a dedicated rack is reserved for calibration, after a calibration test has been placed and completed, the same rack may be…
Class IIFDA: OngoingBeckman Coulter Mishima K.K.
FoodAug 7, 2024
Natural Organics NaturesPlus T-MALE Liquid Testosterone Support for Men 8 OZ recall — FDA F-1520-2024
Product is missing the ingredient TongKat Ali and has additional Rhodiola Rosea
Class IIIFDA: TerminatedNatural Organics, Inc.
FoodAug 7, 2024
Urban Outfitters Elin Dessert Plates recall — FDA F-1738-2024
Elevated levels of cadmium in plates
Class IIFDA: TerminatedUrban Outfitters Inc.
FoodAug 7, 2024
Natural Organics NaturesPlus ULTRA T-MALE Maximum Strength Testosterone Boost recall — FDA F-1519-2024
Product is missing the ingredient TongKat Ali and has additional Rhodiola Rosea
Class IIIFDA: TerminatedNatural Organics, Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 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 categoriesOctober 2025455 records · 4 categories