Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
Rucker s Wholesale & Service Co . initiated a voluntary recall on 10/31/2017 of Uncle Buck's and Family Choice Dark Chocolate Peanuts following a supplier's recall due to undeclared…
Product contains undeclared milk
Superpotent Drug: Subpotent Drug. FDA analysis found this product to be Out of Specification for assay which could result in either Subpotent and/or Superpotent tablets.
Failed Impurities/Degradation Specifications.
cGMP Deviations: lack of quality assurance at the API manufacturer.
The inner and outer labels on the product contain incorrect reference number of 9-202-3751DS. According to Northgate Technologies, the resistor in the probe will not allow the mislabeled…
A specific lot of the FlexFlowTM Venous Cannula, 200-200, is being recalled because it is sharper or pointier than expected.
It was discovered a low-level radiation leak that was found on the NSI X-7000 system.
Customers have reported, and an internal investigation has confirmed, occurrences of atypical negative O129R reactions for Enterococcus casseliflavus ATCC)R) 700327(TM) in association with…
Potential for partially incomplete seal of product, impacting sterility.
Intermittent communication between the host system and the Flex Cardio
A custom implant manufactured entirely from titanium for a patient with a nickel allergy was requested by a surgeon. After the device was manufactured and used in the planned surgery, it…
Custom surgical kits were manufactured with part #63310 Catheter Urethral 10FR 16" which were subsequently recalled by CR Bard for a potential sterile barrier breach.
Elute may become colored due to the residual presence of heme group origination from hemoglobin present in whole blood samples as well as dried spot (DBS) samples. This can potentially…
Custom surgical kits contain Aplicare Providone Iodine Prep Pads which were subsequently recalled by Medline Industries for in incorrect expiration date.
The devices have an incorrect firmware configuration.
The recommended storage temperature on the label is incorrect.
An internal analysis on complaints received indicated that the welding process may have been performed sub optimally in the 12 lot # involved , leading to reduced mechanical strength of the…
Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone Cement.
Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone Cement.
After a receiving a customer complaint for incorrect labeling, BD has confirmed that a portion of SPS tubes associated with catalog 364960, lot 6090812 were incorrectly labeled at the case…
Certain lots of the Harvest Graft Delivery System GDP-10 Procedure Packs may have a lack of a seal on the inner pouch.
The product has a non-conformity that may cause clips to mislead, jam or fall out of the applier.
Potential for partially incomplete seal of product, impacting sterility.
Browse recent months with enough recall history for useful comparison.
