Safety Recalls
RSS ↗15,379 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 14,601–14,650 of 15,379
- Class I
Food Recall · December 7, 2023
Herold's Salads - Black Bean and Corn Salsa packaged in 12oz, 1lb, 2lb, and 5lb plastic containersPotential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Herold's Salad - Macaroni Salad (Elbow) packaged in 8oz, 12oz, 1lb, 2lb, 5lb, and 10lb plastic containersPotential contamination with Listeria monocytogenes
- Class II
Medical Device Recall · December 7, 2023
Incisive CT, Model Numbers 728144 and 728143. Computed Tomography X-Ray System PIM cable part number 459801179871If the Patient Interface Monitor (PIM) Cable is plugged/unplugged frequently as part of daily operation, the connector and wire may disconnect from the welding point, which may result in intermittent loss of the ECG signal. Loss of ECG signal may lead to the decision to rescan the patient or delay in diagnosis during a clinical emergency.
- Class I
Food Recall · December 7, 2023
Herold's Salads - Health Salad packaged in 12oz, 1lb, and 5lb plastic containersPotential contamination with Listeria monocytogenes
- Class II
Medical Device Recall · December 7, 2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Azurion 5M12, Model Numbers: 722227 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software keyDuring the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.
- Class II
Medical Device Recall · December 7, 2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Azurion 7M20, Model Numbers: 722079, 722224 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software keyDuring the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.
- Class I
Food Recall · December 7, 2023
Herold's Salads - Southern Potato Salad with egg packaged in 12oz, 1lb, 2lb, 3lb, 5lb, and 10b plastic containersPotential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Dutch Valley -Potato Salad packaged in 1lb, 2lb, 5lb, and 10lb plastic tubs.Potential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Herold's Salad - Santa Fe Pasta packaged in 1lb, 2lb, and 5lb plastic containersPotential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Corky's & Lenny's - Potato Salad packaged in 30lb plastic containersPotential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Herold's Salad - Shell Macaroni Salad packaged in 1lb, 2lb, and 5lb plastic containersPotential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Amish Wedding - Rotini Garden Medley packaged in 1lb, 2lb, and 5lb plastic containersPotential contamination with Listeria monocytogenes
- Class II
Medical Device Recall · December 7, 2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Azurion 3M15, Model Numbers: 722064, 722222 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software keyDuring the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.
- Class II
Medical Device Recall · December 7, 2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Azurion 7B20/15, Model Numbers: 722068, 722226 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software keyDuring the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.
- Class I
Food Recall · December 7, 2023
Cleveland's Own - Macaroni Salad (Elbow) - packaged in 5lb and 10lb plastic containersPotential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Herold's Salad - Poppyseed Bowtie Pasta packaged in 1lb, 2lb, 3lb, and 5lb plastic containersPotential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Herold's Salads - Greek Gemelli Pasta Salad packaged in 12oz, 1lb, 2lb, and 5lb plastic containersPotential contamination with Listeria monocytogenes
- Unclassified
Vehicle Recall · December 7, 2023
Toyota Motor Engineering & Manufacturing
2023 TOYOTA TACOMA, 2023 TOYOTA COROLLA, 2023 TOYOTA HIGHLANDER, 2023 TOYOTA HIGHLANDER HYBRID, 2023 TOYOTA COROLLA CROSS HYBRID, 2023 TOYOTA COROLLA CROSS, 2024 LEXUS NX HYBRIDA deactivated driver's air bag that does not deploy as intended increases the risk of injury during a crash.
- Class I
Food Recall · December 7, 2023
Cleveland's Own - Shell Macaroni Salad packaged in 10b plastic containersPotential contamination with Listeria monocytogenes
- Unclassified
Vehicle Recall · December 7, 2023
2023 POLESTAR POLESTAR 2The control arm disconnecting from the steering knuckle can cause a loss of steering, increasing the risk of a crash.
- Class II
Medical Device Recall · December 7, 2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Azurion 5M20, Model Numbers: 722228 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software keyDuring the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.
- Class II
Medical Device Recall · December 7, 2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Azurion 7B12/12, Model Numbers: 722067, 722225 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software keyDuring the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.
- Class III
Food Recall · December 7, 2023
Brand Name: SUPREX Plant Based Nutrition. Product Name: Carb & Sugar Block. Product Size: 120 Vegetable Cellulose Capsules per bottle. Container description: White Plastic Bottle 300CC with white capFDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared.
- Class I
Food Recall · December 7, 2023
Cleveland's Own - Original Potato Salad packaged in 10lb plastic containersPotential contamination with Listeria monocytogenes
- Class II
Medical Device Recall · December 7, 2023
Cobalt XT DR MRI SureScan Implantable Cardioverter Defibrillator, product number DDPA2D1During internal review of Polaris battery assembly data from the HiPot operation, a test systems engineer noticed that some batteries had gone through the High Potential test twice. This was able to occur because the test screen did not prevent retesting after a failure. Some batteries were therefore retested and passed.
- Class I
Food Recall · December 7, 2023
Dutch Valley -Macaroni Salad packaged in 1lb, 2lb, 5lb, and 10lb plastic tubs.Potential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Amish Wedding - Southern Potato Salad with egg packaged in 12oz, 1lb, 2lb, 3lb, 5lb, and 10b plastic containersPotential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Herold's Salads - Rainbow Rotini packaged in 1lb, 2lb, and 5lb plastic containersPotential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Herold's Salads - Crab Dip packaged in 12oz, 1lb, 2lb, and 5lb plastic containersPotential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Herold's Salad -Macaroni Salad packaged in 1lb, 2lb, 5lb, and 10lb plastic tubs.Potential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Herold's Salad - Southern Macaroni Salad packaged in 1lb, 2lb, 3lb, 5lb, and 10b plastic containersPotential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Amish wedding -Macaroni Salad packaged in 12oz, 1lb, 5lb, and 10lb plastic tubs.Potential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Herold's Salads - Southern Potato Salad packaged in 12oz, 1lb, 2lb, 3lb, 5lb, and 10b plastic containersPotential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Amish Wedding - Southern Macaroni Salad packaged in 1lb, 2lb, 5lb, and 10b plastic containersPotential contamination with Listeria monocytogenes
- Class II
Medical Device Recall · December 7, 2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Azurion 7M12, Model Numbers: 722078, 722223 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software keyDuring the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.
- Class I
Food Recall · December 7, 2023
Herold's Salads -Potato Salad packaged in 1lb, 2lb, 5lb, and 10lb plastic tubs.Potential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Herold's Salads - Rotini Garden Medley packaged in 1lb, 2lb, and 5lb plastic containersPotential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Amish Wedding -Potato Salad packaged in 12oz and 5lb plastic tubs.Potential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Herold's Salads - Lemon Spring Rotini packaged in 1lb, 2lb, and 5lb plastic containersPotential contamination with Listeria monocytogenes
- Class I
Food Recall · December 7, 2023
Amish Wedding - Cucumber Salad packaged in 12oz, 1lb, 2lb, and 5lb plastic containersPotential contamination with Listeria monocytogenes
- Class II
Medical Device Recall · December 7, 2023
MINC+ Benchtop Incubator, Reference Part Number (RPN) K-MINC-2000, Order Number (GPN) G44429The MINC+ device is susceptible to losing temperature control of electrostatic discharge (static electricity) is applied to the lid of the device. This may lead to embryo degeneration necessitating an additional medical procedure for the patient.
- Class II
Medical Device Recall · December 7, 2023
Terragene Bionova PCD (PCD222-C)Due to a discrepancy between the FDA-Cleared Indications for Use (IFU) and the actual IFU distributed with the products.
- Class II
Medical Device Recall · December 7, 2023
Terragene Integron IT26-C Terragene Integron IT26-C with extender Benco Dental Chemical Integrator [5726-583] Tuttnauer (WTL198-0082) Terragene Integron (PCD26-C) Terragene Bionova PCDDue to a discrepancy between the FDA-Cleared Indications for Use (IFU) and the actual IFU distributed with the products.
- Class II
Medical Device Recall · December 6, 2023
Baxter Vascular Probe, Product Codes: a) 7081015: 8CM, 1- 1.5 MM GLOBAL, b) 7081520: 8CM, 1.5-2 MM GLOBAL, c) 7082025: 8CM, 2-2.5 MM GLOBAL, d) 7151015: 15CM, 1-1.5 MM GLOBAL, e) 71Cardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the products Instructions for Use (IFU) or Prescribing Information (PI).
- Class II
Medical Device Recall · December 6, 2023
Baxter Ostene Hemostasis Material, Product Codes: a) 1503831, 3.5 G; b) 1503832, 2.5 G; c) 1503833, 1.0 GCardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the products Instructions for Use (IFU) or Prescribing Information (PI).
- Class III
Food Recall · December 6, 2023
Milk N Cookies Keto Brick / 1 Brick, 145g 5.1 ozUndeclared MCT Powder (MCT oil, acacia fiber)
- Class II
Medical Device Recall · December 6, 2023
Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cmThe microcatheter IFU contains an intended use that has not been evaluated by the FDA.
- Class II
Medical Device Recall · December 6, 2023
Baxter FloSeal Hemostatic Matrix RECOTHROM, Product Codes: a) ADS202105, 5mL-6 PK US b) ADS202110, 10mL USCardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the products Instructions for Use (IFU) or Prescribing Information (PI).
- Class II
Medical Device Recall · December 6, 2023
Accure Laser System, Model: PFMS00004Laser system's spot tracking system may become misaligned resulting in the possible risk of delivery of higher-than-expected laser energy to epidermal tissue, which may cause blistering.
- Class II
Medical Device Recall · December 6, 2023
Peri-Guard Repair Patch, Product Codes: a) PC1016NBIO: 10X16CMUS, b) PC1225NBIO: 12X25CMUS, c) PC0404NBIO: 4X4CMUS, d) PC0608NBIO: 6X8CMUS, e) PC0814NBIO: 8X14CMUSCardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the products Instructions for Use (IFU) or Prescribing Information (PI).