Safety Recalls
RSS ↗15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 6,051–6,100 of 15,271
- Class II
Medical Device Recall · June 16, 2025
MEDLINE INDUSTRIES, LP - Northfield
SwabFlush Prefilled Syringe with ICU Medical SwabCaps, 10mL Model no. EMZE010301SwabFlush syringes are affected by the ICU Medical recall of their SwabCap Disinfecting Cap due to a manufacturing issue which affects the seal between the foil lid and plastic container of the Swab Cap. The issue may result in a reduced level of disinfection of the luer access valve, potentially resulting in patient infection/sepsis.
- Class I
Food Recall · June 16, 2025
Needle Mushrooms, Product of China, 200 gram packages, Plastic clear packaging on top with blue on the bottom (non-transparent). 25 packages per box .Product tested positive for L. monocytogenes .
- Class II
Medical Device Recall · June 16, 2025
BD PhaSeal Injector Luer (N30C), REF: 515001 BD PhaSeal Injector Luer Lock (N35), REF: 515003 BD PhaSeal Injector Luer Lock (N35C), REF: 515004 BD PhaSeal Injector Lu63er Lock (N35C Multi), REF: 51Closed system drug transfer devices were shipped to the U.S. market without a U.S. version of the instructions for use, which could be an issue if a healthcare professional is prompted to review it.
- Class I
Medical Device Recall · June 16, 2025
HME TwinStar HEPA Plus Filter. Bidirectionally breathing system filter.Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.
- Class I
Food Recall · June 16, 2025
47518 - Nonpareil, Semi-Sweet Chocolate (Christmas Seeds), 25lb Bulk Cases Packaged into Various Size Units After distribution.undeclared milk allergen
- Class I
Food Recall · June 16, 2025
Weaver Chocolates, D2645 - Nonpareil, Semi-Sweet Chocolate (White Seeds) - 25 lbs. Bulk CasesUndeclared Milk Allergen
- Class I
Food Recall · June 16, 2025
Weaver Chocolates, 47518 - Nonpareil, Semi-Sweet Chocolate (Christmas Seeds) - 25 lbs. Bulk CasesUndeclared Milk Allergen
- Class II
Food Recall · June 14, 2025
Wegmans brand Mini Muffins; CHOCOLATE CHIP; NET WT 13.5 OZ; packaged in plastic clamshell; UPC 7789053223Product may contain foreign objects of metal origin.
- Class II
Food Recall · June 14, 2025
Wegmans brand Mini Muffins; Blueberry; NET WT 20 OZ (1 LB 4 OZ) 567 g; FAMILY PACK; packaged in plastic clamshell; UPC 7789053227Product may contain foreign objects of metal origin.
- Class II
Food Recall · June 14, 2025
a. Wegmans brand Mini Muffins; FRENCH TOAST; NET WT 22 OZ (1 LB 6 OZ) 624 g; FAMILY PACK; packaged in plastic clamshell; UPC 7789058612 b. Wegmans brand Mini Muffins; FRENCH TOAST; NET WT 13 OZ (369Product may contain foreign objects of metal origin.
- Class II
Food Recall · June 13, 2025
Crown Point Shelled Edamame, net wt. 22lbs. UPC 813973 01840 4. Product is packaged in carton box with poly liner. Distributed by Alpine Foods Distributing Inc. Milwaukie, OR. Product of China.Label declares Shelled Edamame but does not specify or declare soy.
- Class II
Food Recall · June 13, 2025
vitamins B12 dietary supplement Raspberry Flavored sold under the following brand names: 1. Black Girl Vitamins 60 gummies UPC 8 60008 57505 0 Manufactured for: Black Girl Vitamins 601 W Harrison SUndeclared Peanuts. The firm was notified by their supplier, that the product may contain undeclared peanuts.
- Class I
Food Recall · June 13, 2025
Cucumbers Box 40Lbs 1 1/9 Bushels.Cucumbers have the potential to be contaminated with Salmonella
- Class II
Medical Device Recall · June 13, 2025
Volcano Visions Digital IVUS Catheter: PV.014P (Platinum), REF:85910P; PV.014P RX, REF: 014R; and PV.018, REF: 86700, 86700J used with Instructions for use.Reports of IVUS catheter and guide wire entanglement during radial-to-peripheral procedures, due to catheter use without appropriate sheath and/or guide catheter, which may require further intervention, such as surgical removal; Firm is restating instructions for use and adding: "Use a guide sheath of appropriate length to provide adequate support to the rapid exchange IVUS catheter and guidewire"
- Class II
Medical Device Recall · June 12, 2025
Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD42 Model/Catalog Number: 952-28-42F Software Version: NA Product Description: The EMPOWR DuaDue to packaging discrepancy with the incorrect tibial inserts/implants being packaged. Issued discovered via a customer complaint.
- Class II
Medical Device Recall · June 12, 2025
Estrone RIA Catalog Number DSL8700 UDI Code: 15099590211615 Estrone RIA is an in vitro diagnostic manual medical device used by healthcare professionals for the quantitative measurement of estroneEstrone RIA kit lots may rarely give falsely high patient results which might cause Temporary injury of Remote probability or rarely give falsely low patient results which might cause Permanent injury of Remote probability. Only in some (very rare) cases may the issue occur.
- Class II
Medical Device Recall · June 12, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: C-SECTION PREP, REF DYNJ32702BAffected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in turn lead to the infection related harms for the patient.
- Class II
Medical Device Recall · June 12, 2025
Johnson & Johnson Vision Care, Inc.
ACUVUE¿ OASYS MAX 1-Day MULTIFOCALDue to defects (bubbles/voids) identified during standard finished goods testing
- Unclassified
Consumer Product Recall · June 12, 2025
Anker Innovations Limited, of China
Anker PowerCore 10000 power banks (model A1263 only)The lithium-ion battery in the power bank can overheat, posing fire and burn hazards to consumers.
- Unclassified
Consumer Product Recall · June 12, 2025
TI Outdoor Power Equipment Inc., of Anderson, South Carolina
RYOBI 40V 24-Inch Cordless Hedge TrimmersThe hedge trimmer blade can unexpectedly activate after pressing just the safety or trigger control individually rather than engaging the safety and trigger controls simultaneously, posing a laceration hazard.
- Class II
Medical Device Recall · June 12, 2025
Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD40 Model/Catalog Number: 952-28-40E Software Version: NA Product Description: The EMPOWR DuaDue to packaging discrepancy with the incorrect tibial inserts/implants being packaged. Issued discovered via a customer complaint.
- Class II
Medical Device Recall · June 12, 2025
Estrone RIA, REF: DSL8700. Estrone RIA is an IVD used for the quantitative measurement of estrone in human serum and plasma.A specific lot of bovine serum albumin (BSA) used for manufacturing of coated tubes (CT) that are included in the Estrone RIA kit lots caused different affinity of manufactured coated tubes to patient samples, causing falsely increased assay results for the impacted Estrone RIA kits.
- Class II
Medical Device Recall · June 12, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: 1) BLOOD CULTURE KIT, REF DYNDH1462B; 2) BLOOD CULTURE KIT, REF DYNDH1622C; 3) BLOOD CULTR KT DIVRSN DEVICAffected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in turn lead to the infection related harms for the patient.
- Unclassified
Consumer Product Recall · June 12, 2025
Agro Superior Group LLC, of Princeton, New Jersey
Oliver & Smith 6-inch MattressesThe recalled mattresses violate mandatory flammability standards for mattresses, posing a fire hazard and risk of serious injury or death to consumers.
- Class II
Medical Device Recall · June 12, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: IV START KIT LAB DRAW-SH, REF CDS860014PAffected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in turn lead to the infection related harms for the patient.
- Class II
Medical Device Recall · June 12, 2025
Ortho-Clinical Diagnostics, Inc.
VITROS Chemistry Products OP Reagent Gen 15. Model Number: 680 1997. The VITROS OP Reagent is a dual-chambered package containing ready-to-use liquid reagents that are used to detect opiates in urine.Lots from Generation (GEN) 15 of VITROS Chemistry Products OP Reagent may generate lower than expected quality control (QC) results. If the customer is unable to get passing quality control results, then the customer would be unable to run the OP-LO protocol leading to a potential delay in patient results.
- Class II
Medical Device Recall · June 12, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: LABOR TRIAGE KIT, REF DYKM1564Affected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in turn lead to the infection related harms for the patient.
- Class II
Medical Device Recall · June 12, 2025
Bridge to Life EasiSlush, (Sodium Chloride Solution for Sterile Slush Preparation) (0.9% Sodium Chloride Irrigation, USP), Part Number REF BTLE-1250The firm issued a field safety notice after becoming aware of three lots of products not having quarterly dose audits being completed on time in the first quarter of 2024. Routine lot by lot testing was completed properly however the quarterly dose audit (sampling/testing to monitor the gamma sterilization process and confirm the validated parameters remain effective to assure sterility and bioburden reduction per requirements) was not completed on time.
- Unclassified
Consumer Product Recall · June 12, 2025
Bugaboo North America Inc., of New York
Giraffe highchairsThe highchairs pose a fall hazard and risk of serious injury or death to babies because the legs of the chair can detach from the frame if the screws connecting the legs are not properly tightened during assembly.
- Unclassified
Consumer Product Recall · June 12, 2025
Endless Pools, of Aston, Pennsylvania
Manual Retractable Security Pool CoversThe recalled pool covers can leave a gap of more than 4.5 inches between the cover roller and the pool surface, when installed incorrectly by the installer. An improper installation can result in the covers not conforming to the voluntary industry standard, ASTM F-1346, posing drowning and entrapment hazards to children that could result in serious injury or death.
- Unclassified
Consumer Product Recall · June 12, 2025
Mammut Sports Group Inc., of Williston, Vermont
Skywalker Pro Via Ferrata Sets, Skywalker Pro Turn Via Ferrata Sets and Skywalker Pro Via Ferrata PackagesThe carabiner can be opened without engaging the safety latch, posing a risk of serious injury or death due to fall hazard.
- Class II
Medical Device Recall · June 11, 2025
PARTIAL NEPHRECTOMY - ROBOTIC. Medical convenience kit.CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- Unclassified
Vehicle Recall · June 11, 2025
2023 JEEP GRAND CHEROKEE 4XE, 2024 JEEP GRAND CHEROKEE 4XE, 2025 JEEP GRAND CHEROKEE 4XEA loss of drive power increases the risk of a crash, and a vehicle fire can increase the risk of injury.
- Class II
Medical Device Recall · June 11, 2025
ROBOTIC URO/GYN PACK. Medical convenience kit.CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- Class III
Drug Recall · June 11, 2025
Orient Pharma Co., Ltd. Yunlin Plant
Pitavastatin Tablets, 1 mg, Rx Only, 90 Tablets, Manufactured by: Orient Pharma Co., Ltd., 8 Kehu 1st Road, Huwei Chen, Yunlin, Taiwan, 63247, Manufactured for: Teva Pharmaceuticals, Parsippany, NJ 07Failed Impurities/Degradation Specifications.
- Class II
Medical Device Recall · June 11, 2025
HVI CARDIAC ROBOT PACK. Medical convenience kit.CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- Class III
Drug Recall · June 11, 2025
Famciclovir Tablets, USP 500 mg, 30-count bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc., Manufactured by: Macleods Pharmaceuticals Ltd., Daman, India NDC# 33342-026-07.Presence of Foreign Substance- Black hair strand found attached to a tablet in a sealed bottle.
- Class III
Food Recall · June 11, 2025
LION Pineapple Spring Water Hydration Drink, 20 fl. oz, packaged in PET bottles, packed 12 per casePotential contamination with floating objects
- Class II
Medical Device Recall · June 11, 2025
GENERAL ROBOTIC PACK. Medical convenience kit.CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- Class II
Medical Device Recall · June 11, 2025
LAPAROSCOPIC GYN. Medical convenience kit.CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- Class II
Medical Device Recall · June 11, 2025
HSG Procedure Tray. Model Number: 6050T. The HSG Procedure Tray is for use in hysterosalpingography and sonohysterography procedures.The HSG Procedure Trays and Endosee System Convenience Kits contain non-sterile iodine pouches, however the peel away lid labels incorrectly identify the iodine pouches as sterile.
- Class II
Medical Device Recall · June 11, 2025
CARDIAC ROBOT PACK. Medical convenience kit.CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- Class II
Medical Device Recall · June 11, 2025
DAVINCI UROLOGY. Medical convenience kit.CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- Class III
Food Recall · June 11, 2025
LION Lemon Lime Spring Water Hydration Drink, 20 fl. oz, packaged in PET bottles, packed 12 per casePotential contamination with floating objects
- Class III
Food Recall · June 11, 2025
LION Mixed Berry Spring Water Hydration Drink, 20 fl. oz, packaged in PET bottles, packed 12 per casePotential contamination with floating objects
- Class II
Medical Device Recall · June 11, 2025
GYN ROBOTIC PACK. Medical convenience kit.CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- Class II
Medical Device Recall · June 11, 2025
LAP CHOLE PACK. Medical convenience kit.CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- Class II
Medical Device Recall · June 11, 2025
GYN LAPAROSCOPY PACK. Medical convenience kit.CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- Class II
Medical Device Recall · June 11, 2025
ROBOTIC PROSTATECTOMY PACK. Medical convenience kit.CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.