Latest recalls — page 6
Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 501–600, newest first.
FDA Class II · Medical device · September 23, 2026
When a bolus is included in a treatment plan and sent for secondary dose calculation, the software accounts for it but does not display this clearly, which may lead users to incorr…
Company / brand: PTW FREIBURG recalls
Official ID Z-3174-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
There is a discrepancy between the product identification on the packaging and the dimensions of the implant contained inside.
Company / brand: Straumann USA recalls
Official ID Z-3173-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
The 6Fr suction catheter could not pass through the samples smoothly.
Company / brand: WELL LEAD MEDICAL CO recalls
Official ID Z-3172-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be …
Company / brand: GE Healthcare recalls
Official ID Z-3171-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be …
Company / brand: GE Healthcare recalls
Official ID Z-3170-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be …
Company / brand: GE Healthcare recalls
Official ID Z-3169-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be …
Company / brand: GE Healthcare recalls
Official ID Z-3168-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be …
Company / brand: GE Healthcare recalls
Official ID Z-3167-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be …
Company / brand: GE Healthcare recalls
Official ID Z-3166-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
Potential for oxygen tubing leaks due to failure of the tubing or tubing connection, which may lead to oxygen desaturation.
Company / brand: NOXBOX recalls
Official ID Z-3165-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
Due to a software issue
Company / brand: Nuclein recalls
Official ID Z-3164-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…
Company / brand: ICU Medical recalls
Official ID Z-3163-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…
Company / brand: ICU Medical recalls
Official ID Z-3162-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…
Company / brand: ICU Medical recalls
Official ID Z-3161-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…
Company / brand: ICU Medical recalls
Official ID Z-3160-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…
Company / brand: ICU Medical recalls
Official ID Z-3159-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…
Company / brand: ICU Medical recalls
Official ID Z-3158-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…
Company / brand: ICU Medical recalls
Official ID Z-3157-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…
Company / brand: ICU Medical recalls
Official ID Z-3156-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 2026
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.
Company / brand: AVID Medical recalls
Official ID Z-3154-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 2026
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.
Company / brand: AVID Medical recalls
Official ID Z-3153-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 2026
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.
Company / brand: AVID Medical recalls
Official ID Z-3152-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 2026
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.
Company / brand: AVID Medical recalls
Official ID Z-3151-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 2026
The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly.
Company / brand: Abiomed recalls
Official ID Z-3150-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 2026
The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly.
Company / brand: Abiomed recalls
Official ID Z-3149-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 2026
The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly.
Company / brand: Abiomed recalls
Official ID Z-3148-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
Some devices may not have been properly sterilized due to a manufacturing sterilization issue.
Company / brand: Bayer Medical Care recalls
Official ID Z-3147-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
The packaging may not consistently maintain sterile barrier integrity.
Company / brand: Maquet Cardiopulmonary recalls
Official ID Z-3146-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
The packaging may not consistently maintain sterile barrier integrity.
Company / brand: Maquet Cardiopulmonary recalls
Official ID Z-3145-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
The packaging may not consistently maintain sterile barrier integrity.
Company / brand: Maquet Cardiopulmonary recalls
Official ID Z-3144-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 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.
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-3143-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
Due to software malfunction, patient information system may freeze and become unresponsive.
Company / brand: Philips North America recalls
Official ID Z-3142-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
Due to software malfunction, patient information system may freeze and become unresponsive.
Company / brand: Philips North America recalls
Official ID Z-3141-2026 ·
Official record ↗
FDA Class II · Medical device · September 23, 2026
The kits contain a Retrograde Coronary Sinus Perfusion (RCSP) cannulae that has the potential for a sterile barrier breach. Sterility of the product cannot be assured. If a comprom…
Company / brand: Medline Industries recalls
Official ID Z-3137-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 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 i…
Company / brand: Nova Biomedical recalls
Official ID Z-3132-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 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 i…
Company / brand: Nova Biomedical recalls
Official ID Z-3131-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 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 i…
Company / brand: Nova Biomedical recalls
Official ID Z-3130-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 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 i…
Company / brand: Nova Biomedical recalls
Official ID Z-3129-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 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 i…
Company / brand: Nova Biomedical recalls
Official ID Z-3128-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 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 Aspergillu…
Company / brand: Medline Industries recalls
Official ID Z-3127-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 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 Aspergillu…
Company / brand: Medline Industries recalls
Official ID Z-3126-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 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 Aspergillu…
Company / brand: Medline Industries recalls
Official ID Z-3125-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 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 Aspergillu…
Company / brand: Medline Industries recalls
Official ID Z-3124-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 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 Aspergillu…
Company / brand: Medline Industries recalls
Official ID Z-3123-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 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 Aspergillu…
Company / brand: Medline Industries recalls
Official ID Z-3122-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 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 Aspergillu…
Company / brand: Medline Industries recalls
Official ID Z-3121-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 2026
Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides
Company / brand: AVID Medical recalls
Official ID Z-3108-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 2026
Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance.
Company / brand: BD SWITZERLAND SARL recalls
Official ID Z-3080-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 2026
this is a downstream recall of class I recall RES 98777
Company / brand: Bard Access Systems recalls
Official ID Z-2985-2026 ·
Official record ↗
FDA Class I · Medical device · September 23, 2026
this is a downstream recall of class I recall RES 98777
Company / brand: Bard Access Systems recalls
Official ID Z-2984-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
The firm was notified by their Brie Cheese supplier that sample results revealed the presence of Listeria monocytogenes.
Company / brand: Optimus d/b/a/ Markys Caviar recalls
Official ID H-1388-2026 ·
Official record ↗
FDA Class III · Food · September 23, 2026
Unapproved dye Ponceau 4R
Company / brand: Tiffany Food recalls
Official ID H-1387-2026 ·
Official record ↗
FDA Class II · Food · September 23, 2026
Peanuts & Eggs. The firm list peanuts in the ingredient statement but omitted them from the contain statement. They also have eggs listed in the contain statement but there are no …
Company / brand: Best Friends Bakery recalls
Official ID H-1386-2026 ·
Official record ↗
FDA Class II · Food · September 23, 2026
Carrot decoration contains Yellow #5 and Yellow #6 which is not listed on finished product label.
Company / brand: Elegant Foods recalls
Official ID H-1385-2026 ·
Official record ↗
FDA Class II · Food · September 23, 2026
Undeclared sulfites
Company / brand: Elegant Foods recalls
Official ID H-1384-2026 ·
Official record ↗
FDA Class II · Food · September 23, 2026
Undeclared sulfites
Company / brand: Elegant Foods recalls
Official ID H-1383-2026 ·
Official record ↗
FDA Class II · Food · September 23, 2026
The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
Company / brand: Buckhead Meat Company D.B.A. Trinity Seafood recalls
Official ID H-1382-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential E. coli O145:H28 Contamination
Company / brand: Frutas y Hortalizas del Sur recalls
Official ID H-1380-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Jalapenos have the potential to be contaminated with Salmonella
Company / brand: NatureBest Pre-Cut & Produce recalls
Official ID H-1379-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Jalapenos have the potential to be contaminated with Salmonella
Company / brand: NatureBest Pre-Cut & Produce recalls
Official ID H-1378-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Jalapenos have the potential to be contaminated with Salmonella
Company / brand: NatureBest Pre-Cut & Produce recalls
Official ID H-1377-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Jalapenos have the potential to be contaminated with Salmonella
Company / brand: NatureBest Pre-Cut & Produce recalls
Official ID H-1376-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Jalapenos have the potential to be contaminated with Salmonella
Company / brand: NatureBest Pre-Cut & Produce recalls
Official ID H-1375-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Jalapenos have the potential to be contaminated with Salmonella
Company / brand: NatureBest Pre-Cut & Produce recalls
Official ID H-1374-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Jalapenos have the potential to be contaminated with Salmonella
Company / brand: NatureBest Pre-Cut & Produce recalls
Official ID H-1373-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Jalapenos have the potential to be contaminated with Salmonella
Company / brand: NatureBest Pre-Cut & Produce recalls
Official ID H-1372-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1368-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1367-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1366-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1365-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1364-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1363-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1362-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1361-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1360-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1359-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1358-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1357-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1356-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1355-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1354-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1353-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1352-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1351-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1350-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1349-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1348-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1347-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1346-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1345-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential contamination with Salmonella.
Company / brand: Taylor Fresh Foods recalls
Official ID H-1344-2026 ·
Official record ↗
FDA Class II · Food · September 23, 2026
Undeclared peanuts
Company / brand: Quality Dairy Farms recalls
Official ID H-1343-2026 ·
Official record ↗
FDA Class II · Food · September 23, 2026
Product may be contaminated with Salmonella
Company / brand: Panorama Produce Sales recalls
Official ID H-1342-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Sprouts may be contaminated with STEC E. coli and/or Salmonella.
Company / brand: Everything Sprouts recalls
Official ID H-1340-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Sprouts may be contaminated with STEC E. coli and/or Salmonella.
Company / brand: Everything Sprouts recalls
Official ID H-1339-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Sprouts may be contaminated with STEC E. coli and/or Salmonella.
Company / brand: Everything Sprouts recalls
Official ID H-1338-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Sprouts may be contaminated with STEC E. coli and/or Salmonella.
Company / brand: Everything Sprouts recalls
Official ID H-1337-2026 ·
Official record ↗
FDA Class I · Food · September 23, 2026
Potential Salmonella contamination
Company / brand: FOODS ALIVE recalls
Official ID H-1336-2026 ·
Official record ↗
FDA Class I · Drug · September 23, 2026
Superpotent Drug
Company / brand: VITRUVIAS THERAPEUTICS recalls
Official ID D-0866-2026 ·
Official record ↗
FDA Class II · Drug · September 23, 2026
Lack of Assurance of Sterility
Company / brand: Pfizer recalls
Official ID D-0853-2026 ·
Official record ↗
Official sources
Government sources last checked October 22, 2026 at 12:00 PM UTC.