Complete FDA and NHTSA recall records dated in July 2024.
These records include useful source details for the selected month.
Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder.
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime,…
The duration between the implantable pulse generator reaching the elective replacement indicator threshold and end of service may be shorter than indicated in product labeling.
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime,…
After surgery initiation, while using surgical image guidance, if significant eye rotation/movement occurs, a software anomaly may cause re-establishment of incorrect new registration…
Potential under-processing.
Product may contain foreign object that appears to be of rodent origin.
Potential under-processing.
Product may be contaminated with Listeria monocytogenes.
Product may be contaminated with Listeria monocytogenes.
Potential under-processing.
Product may be contaminated with Listeria monocytogenes.
The product's glass bottle may be prone to breakage
Potential under-processing.
Potential under-processing.
Undeclared allergen - hazelnuts
Potential under-processing.
Product may be contaminated with Listeria monocytogenes.
Potential under-processing.
Potential under-processing.
Product contains elevated levels of undeclared sulfites.
Potential under-processing.
Product may be contaminated with Listeria monocytogenes.
Potential under-processing.
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.
