FoodSep 16, 2020
Treehouse Foods Signature Select Chewy Granola Bars, Chocolate Chip, Family recall — FDA F-1424-2020
Product may contain undeclared peanut butter.
Class IFDA: TerminatedTreehouse Foods
September 2020 recalls — page 7
These records include useful source details for the selected month.
FoodSep 16, 2020
HELLOFRESH US Various HelloFresh and EveryPlate meal kits containing onions recall — FDA F-1428-2020
Onions included various meal kits may be contaminated with Salmonella.
Class IFDA: TerminatedHELLOFRESH US
FoodSep 16, 2020
Power Selles Imports dba Culinary Collective Blanxart 82% Congo Organic Chocolate Bar recall — FDA F-1425-2020
A foreign object found by a consumer in a chocolate bar.
Class IIFDA: TerminatedPower Selles Imports dba Culinary Collective
FoodSep 16, 2020
Preferred Popcorn Organic Yellow Popcorn packaged in the following ways: 1) recall — FDA F-1437-2020
Popcorn may contain foreign material: tempered glass between 3 mm and 7 mm in size
Class IIFDA: TerminatedPreferred Popcorn
FoodSep 16, 2020
Ingredients Solutions MBF-202 Carrageenan recall — FDA F-1435-2020
On August 28, 2020, the firm's customer discovered colored fibers up to 1/4 " in length after sifting a lot of finished carrageenan intended for use as an ingredient in a finished food…
Class IIFDA: TerminatedIngredients Solutions Inc.
FoodSep 16, 2020
B&G Foods Back to Nature, Organic Rosemary and Olive Oil Stoneground recall — FDA F-1429-2020
The product contains undeclared milk.
Class IIFDA: TerminatedB&G Foods North America, Inc.
FoodSep 16, 2020
Kader Exports Pvt Cooked, Peeled and Deveined, Tail-on, Shrimp recall — FDA F-1432-2020
Frozen cooked shrimp is possibly contaminated with Salmonella.
Class IIFDA: TerminatedKader Exports Pvt. Ltd.
FoodSep 16, 2020
The Superior Nut Company SOUTHERN GROVE recall — FDA F-1434-2020
Product contains undeclared brazil nuts.
Class IIFDA: TerminatedThe Superior Nut Company, Inc.
DrugSep 16, 2020
Maquiladora Miniara Sa De Cv Shine & Clean Hand Sanitizer gel, (Ethyl Alcohol 70%), 33.81 fl recall — FDA D-1565-2020
CGMP Deviations: Products manufactured at the same site were FDA testing found below the label claim for ethanol content and the presence of undeclared methanol.
Class IIFDA: TerminatedMaquiladora Miniara Sa De Cv
DrugSep 16, 2020
Cephalexin for Oral Suspension, USP 250 mg per 5 mL, For Reconstitution, For Oral Use Only recall — FDA D-1566-2020
Sub-Potent Drug: Out of specification test results for potency (below specification).
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugSep 16, 2020
Open Book Extracts Always Be Clean Hand Sanitizer (73% Alcohol) 0.04 FL OZ (1.2 mL) recall — FDA D-1563-2020
Labeling Not Elsewhere Classified: Product labeled to contain methanol
Class IIFDA: TerminatedOpen Book Extracts
DrugSep 16, 2020
Cephalexin for Oral Suspension, USP 125 mg per 5 mL, For Reconstitution, For Oral Use Only recall — FDA D-0012-2021
CGMP deviations; there is a possibility that some bottles in these lots may have the active ingredient above and/or below specification limits.
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugSep 16, 2020
Cephalexin for Oral Suspension, USP 250 mg per 5 mL, For Reconstitution, For Oral Use Only recall — FDA D-0013-2021
CGMP deviations; there is a possibility that some bottles in these lots may have the active ingredient above and/or below specification limits.
Class IIFDA: TerminatedTeva Pharmaceuticals USA
VehicleSep 10, 2020
Ford automatic transmission recall — NHTSA campaign 20V550000
Ford Motor Company (Ford) is recalling certain 2019-2020 Edge, Transit Connect and Lincoln MKX and 2020 Escape and Lincoln Corsair vehicles. The start/stop accumulator endcap may have…
automatic transmissionFord Motor Company
VehicleSep 10, 2020
Explorer buckle recall — NHTSA campaign 20V549000
Ford Motor Company (Ford) is recalling certain 2020 Explorer vehicles. The affected vehicles are equipped with second row center seat belt buckles that may not be properly secured to the…
buckleFord Motor Company
VehicleSep 10, 2020
Chrysler camera recall — NHTSA campaign 20V191000
Chrysler (FCA US LLC) is recalling certain 2020 Jeep Gladiator and Jeep Cherokee, 2019-2020 Ram 1500 Pickup, Ram 2500 Pickup, Ram 3500 Pickup, Chrysler Pacifica, Dodge Durango, Jeep Grand…
cameraChrysler (FCA US LLC)
Medical DeviceSep 9, 2020
C.A. Greiner & Sohne Gesellschaftmbh Plastic Cannula HOLDEX Item # 450216 - Product Usage recall — FDA Z-2911-2020
Sample leaking from the sleeve covering the needle inside the cannula
Class IIFDA: OngoingC.A. Greiner & Sohne Gesellschaftmbh
Medical DeviceSep 9, 2020
Cardinal Health 200 PROTEXIS Latex Micro Surgical Gloves Size 6.5 - Product Usage: This recall — FDA Z-2914-2020
A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
Class IIFDA: CompletedCardinal Health 200, LLC
Medical DeviceSep 9, 2020
Cardinal Health 200 PROTEXIS Latex Micro Surgical Gloves Size 7.0 - Product Usage: This recall — FDA Z-2915-2020
A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
Class IIFDA: CompletedCardinal Health 200, LLC
Medical DeviceSep 9, 2020
RANDOX LABORATORIES Pancreatic Amylase AY3855 batch 480483 Pancreatic Amylase Ethylidene recall — FDA Z-2924-2020
Amylase AY3805 batch 480449 and Pancreatic Amylase AY3855 batch 480483 have failed to meet the quoted performance claims prior to expiry on 28th Sept 2020.
Class IIFDA: TerminatedRANDOX LABORATORIES, LTD.
Medical DeviceSep 9, 2020
TELEFLEX MEDICAL Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is recall — FDA Z-2922-2020
Potential sterility issue
Class IIFDA: TerminatedTELEFLEX MEDICAL Inc.
Medical DeviceSep 9, 2020
Stimwave Technologies StimQ Peripheral Nerve Stimulator System (PNS) Model STQ4-SPR-BO US recall — FDA Z-2932-2020
The product contains a non-functional component not referenced in product labeling.
Class IIFDA: OngoingStimwave Technologies Inc.
Medical DeviceSep 9, 2020
Cardinal Health 200 PROTEXIS Latex Micro Surgical Gloves Size 9.0 - Product Usage: This recall — FDA Z-2919-2020
A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
Class IIFDA: CompletedCardinal Health 200, LLC
Medical DeviceSep 9, 2020
CareFusion 303 BD Alaris System. The EtCO2 module is a capnograph indicated for continuous recall — FDA Z-2935-2020
Infusion pump component defect may result in interruption of patient monitoring
Class IIFDA: OngoingCareFusion 303, Inc.
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.