Health & Personal Care
HIGH
FDA DEVICE
Siemens Healthcare Diagnostics Atellica CH A1c_E Recall for 21,291 Units (2026)
Siemens Healthcare Diagnostics
A potential
nhtsa regulated Recalls
370 recalls tagged with “nhtsa regulated”.
Health & Personal Care
HIGH
FDA DRUG
Radnostix Sodium Iodide I-131 Gel Capsule Pack Recalled for 2,699 Units in 2026
SODIUM IODIDE I-131
Failed Tablet/Capsule
Food & Beverages
HIGH
FDA FOOD
Made Fresh Salads Recalls 557 Tofu Whipped 5-lb Tubs Over Listeria Contamination (2026)
Products may be contaminated with Listeria monocytogenes.
Made Fresh Salads
Products may
Food & Beverages
HIGH
FDA FOOD
Made Fresh Salads Recalls 557 Walnut Raisin Cream Cheese 5 lb Tubs Over Listeria Risk (2026)
Products may be contaminated with Listeria monocytogenes.
Made Fresh Salads
Products may
Health & Personal Care
HIGH
FDA DEVICE
Navajo Manufacturing Handy Solutions Neck & Shoulders Heating Pad Recalled 28,457 Units (2026)
Navajo Manufacturing
If heating
Health & Personal Care
HIGH
FDA DEVICE
Medline Sterile Radiology Procedure Kits Recalled for Sterility Breach (2026)
There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.
Medline Industries, LP
There is
Health & Personal Care
HIGH
FDA DEVICE
Mentor Texas Artoura Breast Tissue Expanders Recalled Worldwide Over Dull Infusion Needle Tips (2026
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
Mentor Texas
Infusion sets
Health & Personal Care
HIGH
FDA DRUG
Kirkman MAXIMUM Zone 1 4% Lidocaine Cream Recall 178 Bottles (2026)
Stability Data Does Not Support Expiry Date.
Kirkman
Stability Data
Health & Personal Care
HIGH
FDA DRUG
K Kirkman FIVE-STAR VASOCAINE Spray Recall for Expiry-Date Stability Issue (2026)
Stability Data Does Not Support Expiry Date.
Kirkman
Stability Data
Health & Personal Care
HIGH
FDA DEVICE
Abiomed Impella Automated Controller Recall 62 Units in 2026
Potential that the "Purge System Blocked" alarm display on the Automated Impella Controller (AIC) could be delayed when using first generation Impella 5.5 (0550-0008*) pumps.
Abiomed
Potential that
Health & Personal Care
HIGH
Health & Personal Care
HIGH
FDA DRUG
Harbin Jixianglong Biotech Semaglutide Rx Compounding Recall (2026)
CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution
Harbin Jixianglong Biotech Co.
CGMP Deviations
Health & Personal Care
HIGH
FDA DRUG
Harbin Jixianglong Biotech Semaglutide Rx Compounding Recall 2026 — 6 Packaging Sizes
CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution
Harbin Jixianglong Biotech Co.
CGMP Deviations
Health & Personal Care
HIGH
FDA DEVICE
Olympus OER-Pro Endoscope Reprocessor Recall for 3,354 Units Over MAJ-1443/1444 Compatibility (2026)
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
Olympus Corporation of the Americas
The MAJ-1443
Health & Personal Care
HIGH
FDA DEVICE
Olympus MAJ-1443/MAJ-1444 Endoscope Suction Valves Recalled in 2026
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
Olympus Corporation of the Americas
The MAJ-1443
Health & Personal Care
HIGH
FDA DEVICE
Olympus MAJ-1444 Endoscope Air/Water Valve Recall 2026 for 89,579 Units
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
Olympus Corporation of the Americas
The MAJ-1443
Health & Personal Care
HIGH
FDA DEVICE
Burlington Medical Blockers Recalled for Attenuation Degradation in 51 Units Worldwide (2026)
Potential for attenuation degradation over time, decreasing the lifespan.
Burlington Medical
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Burlington Medical BAT Coverage Recall 1,489 Units Worldwide in 2026
Potential for attenuation degradation over time, decreasing the lifespan.
Burlington Medical
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Reflexion Medical Recalls 12 RefleXion X1 Radiotherapy Systems for Software Defect (2026)
Reflexion Medical
Due to
Health & Personal Care
HIGH
FDA DEVICE
International Life Sciences Recalls Artelon FlexBand Plus Augmentation Devices for Endotoxin Testing
Augmentation devices failed bacterial endotoxin testing.
International Life Sciences
Augmentation devices