The latest food, drug and medical device recalls reported by the U.S. Food and Drug Administration, newest first. Data updated Oct 21, 2026.
87,918 recalls · page 16 of 30
Potential contamination with Salmonella.
Reported Sep 23, 2026 · H-1361-2026
Sprouts may be contaminated with STEC E. coli and/or Salmonella.
Reported Sep 23, 2026 · H-1340-2026
Jalapenos have the potential to be contaminated with Salmonella
Reported Sep 23, 2026 · H-1375-2026
Potential contamination with Salmonella.
Reported Sep 23, 2026 · H-1359-2026
Potential Salmonella contamination
Reported Sep 23, 2026 · H-1336-2026
Potential contamination with Salmonella.
Reported Sep 23, 2026 · H-1344-2026
Potential contamination with Salmonella.
Reported Sep 23, 2026 · H-1367-2026
Potential contamination with Salmonella.
Reported Sep 23, 2026 · H-1345-2026
Undeclared peanuts
Reported Sep 23, 2026 · H-1343-2026
Potential E. coli O145:H28 Contamination
Reported Sep 23, 2026 · H-1380-2026
Potential contamination with Salmonella.
Reported Sep 23, 2026 · H-1353-2026
Sprouts may be contaminated with STEC E. coli and/or Salmonella.
Reported Sep 23, 2026 · H-1337-2026
Failed Stability Specifications
Reported Sep 23, 2026 · D-0845-2026
Failed Stability Specifications
Reported Sep 23, 2026 · D-0846-2026
Failed Stability Specifications
Reported Sep 23, 2026 · D-0844-2026
Superpotent Drug
Reported Sep 23, 2026 · D-0866-2026
Failed Stability Specifications
Reported Sep 23, 2026 · D-0843-2026
Failed Stability Specifications
Reported Sep 23, 2026 · D-0842-2026
Failed Stability Specifications
Reported Sep 23, 2026 · D-0841-2026
Failed Content Uniformity Specifications. Out of Specification for Assay during analysis at the 24- month long term stability station, at (25¿C,60%RH).
Reported Sep 23, 2026 · D-0848-2026
Failed Dissolution Specifications
Reported Sep 23, 2026 · D-0852-2026
Lack of Assurance of Sterility
Reported Sep 23, 2026 · D-0853-2026
Reusable access port system may crack or seperate during use.
Reported Sep 23, 2026 · Z-3183-2026
Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control, the system delivers 100% O2 to the breathing system enabling continued controlled or manual ventilation and initiates audible and visual alarms. When this issue occurs, anesthetic agent delivery will be interrupted and requires clinician intervention. If this is not provided, the patient may experience decreased anesthetic agent effect.
Reported Sep 23, 2026 · Z-3191-2026
Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control, the system delivers 100% O2 to the breathing system enabling continued controlled or manual ventilation and initiates audible and visual alarms. When this issue occurs, anesthetic agent delivery will be interrupted and requires clinician intervention. If this is not provided, the patient may experience decreased anesthetic agent effect.
Reported Sep 23, 2026 · Z-3192-2026
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.
Reported Sep 23, 2026 · Z-3151-2026
The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus penicillioides may lead to serious adverse health consequences, including systemic infection, sepsis, illness, and death.
Reported Sep 23, 2026 · Z-3125-2026
Device may not resume patient monitoring for at least 3 minutes following system restart. Issue can lead to potential delay in recognition of clinically significant events.
Reported Sep 23, 2026 · Z-3143-2026
A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode including patient identification (ID) barcodes and quality control (QC) solution ID barcodes when a new barcode is scanned, resulting in the prior barcode information remaining displayed on the screen for the current test. When this defect occurs and the operator accepts the incorrectly displayed patient information without recognizing the mismatch, the current patient's glucose result will be incorrectly assigned to the previous patient's medical record and transmitted to the data management system (DMS), and the current patient's medical record will not receive a result, leaving their glucose status unrecorded and their clinical management without the information needed to guide treatment decisions. The previous patient, whose medical record now contains a glucose result that does not belong to them, may receive inappropriate clinical intervention based on that erroneous result, particularly in critically ill patients, neonates, and infants who cannot communicate symptoms or self-treat. The defect also affects QC barcode scanning: if a QC scan triggers the same retention behavior, QC results may be attributed to an incorrect identifier or QC tests may fail without the user recognizing the underlying cause. This defect does not affect the analytical accuracy of glucose measurements.
Reported Sep 23, 2026 · Z-3131-2026
Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material within the drip chamber wall that does not enter the fluid path, which if seen by a healthcare provider may lead to replacement of product before use, which could result in a delay in therapy.
Reported Sep 23, 2026 · Z-3159-2026