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.
Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best…
Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not recognize or may misidentify loaded medication syringes. The inability of a pump to recognize a syringe (i.e. the…
Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond during use.
There is the potential for connection failures related to the female two-part luer to hemodialysis blood tubing lines, etc. which may contribute to blood loss or air emboli.
There is the potential for connection failures related to the female two-part luer to hemodialysis blood tubing lines, etc. which may contribute to blood loss or air emboli.
Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best…
Possible Pest Contamination at production facility.
Kraken Kratom, Phytoextractum, and Soul Speciosa WHITE VEIN Kratom CAPSULES are recalled due to potential contamination with Salmonella.
Kraken Kratom, Phytoextractum, and Soul Speciosa products containing Red Vein Kratom Powder are recalled due to potential contamination with Salmonella.
Pumpkin seeds are recalled because the Certificate of Analysis showing a confirmed positive for Listeria species.
Kraken Kratom, Phytoextractum, and Soul Speciosa GREEN VEIN Kratom POWDER are recalled due to potential contamination with Salmonella.
Kraken Kratom, Phytoextractum, and Soul Speciosa products containing WHITE VEIN Kratom Powder are recalled due to potential contamination with Salmonella.
Label did not list sub-ingredients for mayo and sour cream. It contains undeclared egg and milk. The firm found a 2nd PLU which was not corrected. Recall of Weis Dried Beef Party Rye Dip…
Kraken Kratom, Phytoextractum, and Soul Speciosa GREEN VEIN Kratom CAPSULES are recalled due to potential contamination with Salmonella.
Kraken Kratom, Phytoextractum, and Soul Speciosa RED VEin Kratom Capsule are recalled due to potential contamination with Salmonella.
Food & Beverage Inc., dba Chris's Cookies has initiated a recall of Trader Joe s Peanut Butter Sutter s Formula Cookies (Trader Joes SKU 93307) that was packed in a Trader Joes branded…
Failed Impurities/Degradation Specifications: High out of specification results for an impurity.
Lack of Assurance of Sterility: Leakage of the peritoneal dialysis (PD) solution bag.
Defective Container: This recall is being initiated due to product complaints regarding difficulty in dispensing the tablet from the applicator.
Labeling: Label Mix-Up: Brilliant Blue G was labeled with an inaccurate auxiliary label which contained active/inactive ingredient information for incorrect product.
Some of the products listed in the recall may be missing a sticker that contains the lot number, expiration date, and Unique Device Identification (UDI) information.
Contact lenses lack sterility assurance.
The screw in specific lots of the GLOBAL UNITE Anatomic Body and GLOBAL UNITE Fracture Body was inverted during assembly to the body, which will cause the humeral stem to sit proud and may…
The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is…
Browse recent months with enough recall history for useful comparison.
