FoodMay 29, 2024
Geissler's Supermarket Spicy Salmon 9.6 oz Ingredients read in recall — FDA F-1254-2024
undeclared allergens (egg)
Class IFDA: TerminatedGeissler's Supermarket
May 2024 recalls — page 7
These records include useful source details for the selected month.
FoodMay 29, 2024
Geissler's Supermarket Shrimp Tempura and Spicy Shrimp recall — FDA F-1253-2024
undeclared allergens (wheat)
Class IFDA: TerminatedGeissler's Supermarket
FoodMay 29, 2024
Graceleigh, Inc. dba Sammy's Milk Sammy's Milk GOAT MILK TODDLER FORMULA, 0.64oz recall — FDA F-1248-2024
FDA inspection and investigation of firm's website and social media pages found that Sammy's online marketing materials included misleading information that implied the product was safe as…
Class IFDA: TerminatedGraceleigh, Inc. dba Sammy's Milk
FoodMay 29, 2024
Geissler's Supermarket Pink Lady Salmon &Avo Roll Combo recall — FDA F-1252-2024
Undeclared allergens (egg)
Class IFDA: TerminatedGeissler's Supermarket
FoodMay 29, 2024
Reser's Fine Foods Product is MACARONI Salad, but the bottom container is recall — FDA F-1263-2024
Undeclared Wheat. Aldi Macaroni Salad was mislabeled as Coleslaw and Coleslaw label does not declare wheat. Macaroni (pasta) is visible through a clear plastic package.
Class IIFDA: TerminatedReser's Fine Foods, Inc.
FoodMay 29, 2024
Geissler's Supermarket Spicy Tuna recall — FDA F-1255-2024
undeclared allergens (egg)
Class IFDA: TerminatedGeissler's Supermarket
FoodMay 29, 2024
Natural Waters of Viti Fiji Natural Artesian Water 500 mL recall — FDA F-1264-2024
Firm testing revealed Manganese in addition to three bacterial genera.
Class IIIFDA: TerminatedNatural Waters of Viti Limited
FoodMay 29, 2024
Geissler's Supermarket Philadelphia Avo or Cucumber Classic recall — FDA F-1251-2024
undeclared allergens (milk)
Class IIFDA: TerminatedGeissler's Supermarket
DrugMay 29, 2024
niCARdipine Hydrochloride Injection, USP, 25 mg/10 mL (2.5 mg/mL), 10 x 10 mL Single Dose recall — FDA D-0503-2024
Lack of Assurance of Sterility.
Class IIFDA: TerminatedAmerican Regent, Inc.
DrugMay 29, 2024
Haloperidol decanoate Injection 50mg/mL recall — FDA D-0506-2024
Presence of Foreign Substance: This oil based product may contain trace amounts of water for injection (WFI).
Class IIFDA: OngoingSOMERSET THERAPEUTICS LLC
VehicleMay 28, 2024
Tesla warning light/devices recall — NHTSA campaign 24V376000
Tesla, Inc. (Tesla) is recalling certain 2012-2024 Model S, 2015-2024 Model X, 2017-2023 Model 3, and 2020-2023 Model Y vehicles. In the event of an unbelted driver, the seat belt warning…
warning light/devicesTesla, Inc.
Medical DeviceMay 22, 2024
Medtronic Venous Cannulae: a) DLP 20 Fr recall — FDA Z-1805-2024
Potential for unsealed sterile packing.
Class IIFDA: OngoingMedtronic Perfusion Systems
Medical DeviceMay 22, 2024
Boston Scientific Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CLS3 (5PK), REF recall — FDA Z-1677-2024
An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and…
Class IFDA: OngoingBoston Scientific Corporation
Medical DeviceMay 22, 2024
Medtronic Arterial Cannulae packaged as: a) DLP Curved Metal Tip Arterial Cannula 20 Fr. recall — FDA Z-1793-2024
Potential for unsealed sterile packing.
Class IIFDA: OngoingMedtronic Perfusion Systems
Medical DeviceMay 22, 2024
Boston Scientific Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL4 125CM (5PK) recall — FDA Z-1654-2024
An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and…
Class IFDA: OngoingBoston Scientific Corporation
Medical DeviceMay 22, 2024
Boston Scientific Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO JIG4 (5PK), REF recall — FDA Z-1664-2024
An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and…
Class IFDA: OngoingBoston Scientific Corporation
Medical DeviceMay 22, 2024
Boston Scientific Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WR (5PK), REF recall — FDA Z-1672-2024
An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and…
Class IFDA: OngoingBoston Scientific Corporation
Medical DeviceMay 22, 2024
Boston Scientific Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR5 125CM (5PK) recall — FDA Z-1657-2024
An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and…
Class IFDA: OngoingBoston Scientific Corporation
Medical DeviceMay 22, 2024
Boston Scientific Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL3.5 (5PK), REF recall — FDA Z-1653-2024
An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and…
Class IFDA: OngoingBoston Scientific Corporation
Medical DeviceMay 22, 2024
Boston Scientific Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO RCB (5PK), REF recall — FDA Z-1647-2024
An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and…
Class IFDA: OngoingBoston Scientific Corporation
Medical DeviceMay 22, 2024
QUIDELORTHO VITROS Immunodiagnostic Products Free T3 Reagent Pack-IVD is for the recall — FDA Z-1818-2024
T3 Reagent Packs used with Free T3 Calibrators may produce positively biased results for patient and quality control samples. The positive bias may cause erroneous patient results or a…
Class IIFDA: OngoingQUIDELORTHO
Medical DeviceMay 22, 2024
Boston Scientific Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO JIG3.5 (5PK) recall — FDA Z-1663-2024
An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and…
Class IFDA: OngoingBoston Scientific Corporation
Medical DeviceMay 22, 2024
Medtronic Aortic Root Cannulae and Cardioplegia Needles: a) DLP 9 Ga (11 Fr) Aortic Root recall — FDA Z-1800-2024
Potential for unsealed sterile packing.
Class IIFDA: OngoingMedtronic Perfusion Systems
Medical DeviceMay 22, 2024
Boston Scientific Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR3.5 (5PK), REF recall — FDA Z-1638-2024
An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and…
Class IFDA: OngoingBoston Scientific Corporation
How to use this monthly recall archive
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.