Complete FDA and NHTSA recall records dated in November 2019.
These records include useful source details for the selected month.
The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
Users may experience intermittent slide dispense issues with some cartridges due to the anti-backup platen failing to advance inside the cartridge.
Communication error alarms may result in interruption of therapy, delay in therapy, or blood loss due to non-restitution of blood in the extracorporeal circuit.
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
There is a possible assembly error on Autoject EI, lot number V14. This lot was packed into two products: AJ 1310, lot number V14 and AN 3310VET (branded as Petfine Auto Injector), batches…
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
Communication error alarms may result in interruption of therapy, delay in therapy, or blood loss due to non-restitution of blood in the extracorporeal circuit.
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
Device vented gas below the stated pressure.
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
Communication error alarms may result in interruption of therapy, delay in therapy, or blood loss due to non-restitution of blood in the extracorporeal circuit.
Communication error alarms may result in interruption of therapy, delay in therapy, or blood loss due to non-restitution of blood in the extracorporeal circuit.
The assigned value for Rheumatoid Factor over recovers against the reference material RF serum, 1st British standard from NIBSC. Ref = 64/002. The calibrator values have been adjusted to…
Component was not tested by the supplier for adventitious agents
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
Direct Account randomly tested two products with presumptive positive results for Listeria monocytogenes.
The firm received a recall notice for an ingredient, ready-to-eat beef patties, which were potentially contaminated with foreign metal material. The patties were used in the manufacture of…
The firm received a recall notice for an ingredient, ready-to-eat beef patties, which were potentially contaminated with foreign metal material. The patties were used in the manufacture of…
Product is recalled due to a potential for contamination with Listeria monocytogenes.
Product is recalled due to a potential for contamination with Listeria monocytogenes.
FDA sampling found Hepatitis A in frozen raspberries.
Kiwi Strawberry flavored juice beverage has the potential to be contaminated with mold
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.
