FoodJul 24, 2019
Frito-Lay Lay' Lightly Salted Barbecue Flavored Potato Chips Net Wt recall — FDA F-1552-2019
Undeclared milk
Class IFDA: TerminatedFrito-Lay, Inc.
July 2019 recalls — page 22
These records include useful source details for the selected month.
FoodJul 24, 2019
Valley Processing Single Strength Apple Juice shipped in 5700 gallon tanker recall — FDA F-1581-2019
The single strength apple juice is recalled because patulin was found at level greater than 50 ppb.
Class IIFDA: TerminatedValley Processing, Inc.
FoodJul 24, 2019
Pure Ground Ingredients Tea bag Cut 40 lb recall — FDA F-1560-2019
Product tested and found to be positive for Salmonella
Class IFDA: TerminatedPure Ground Ingredients
FoodJul 24, 2019
Commercial Creamery Company of Idaho White Cheddar 5906-KD is a non-GMO White Cheddar Cheese recall — FDA F-1557-2019
White Cheddar Blend is recalled due to a potential contamination with Salmonella.
Class IFDA: TerminatedCommercial Creamery Company of Idaho, Inc.
FoodJul 24, 2019
Sprout's Farmers Market Sprouts Farmers Market Organic Cut Leaf Spinach, Net Wt 16 Oz recall — FDA F-1554-2019
Testing revealed the presence of Listeria monocytogenes in the frozen spinach
Class IIFDA: TerminatedSprout's Farmers Market
FoodJul 24, 2019
Oregon Potato Company Frozen whole Red Raspberries recall — FDA F-1550-2019
Whole Red Raspberries are recalled due to potential contamination with Norovirus.
Class IIFDA: TerminatedOregon Potato Company
FoodJul 24, 2019
Sprout's Farmers Market Sprouts Farmers Market Cut Leaf Spinach, Net Wt 16 Oz recall — FDA F-1553-2019
Testing revealed the presence of Listeria monocytogenes in the frozen spinach
Class IIFDA: TerminatedSprout's Farmers Market
FoodJul 24, 2019
Pure Ground Ingredients Ground 35 lb recall — FDA F-1559-2019
Product tested and found to be positive for Salmonella
Class IFDA: TerminatedPure Ground Ingredients
DrugJul 24, 2019
Fluorouracil Injection, USP, 5 g / 100 mL (50 mg / mL), 100 mL fill in a 100 mL vial recall — FDA D-1489-2019
Presence of Particulate Matter; glass particulates
Class IFDA: TerminatedFresenius Kabi USA, LLC
DrugJul 24, 2019
Pfizer Milrinone Lactate Injection 200 mcg (0.2 mg)/mL* in 5% Dextrose Injection 40 mg/200 recall — FDA D-1486-2019
Lack of Assurance of Sterility: Bags have the potential to leak.
Class IIFDA: TerminatedPfizer Inc.
DrugJul 24, 2019
Lupin Pharmaceuticals Gatifloxacin Ophthalmic Solution 0.5%, For Use in the Eyes Only recall — FDA D-1490-2019
Labeling: Missing label; Product complaints reported missing bottle label.
Class IIIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugJul 24, 2019
Pfizer Milrinone Lactate Injection 200 mcg (0.2 mg)/mL* in 5% Dextrose Injection, 20 mg/100 recall — FDA D-1487-2019
Lack of Assurance of Sterility: Bags have the potential to leak.
Class IIFDA: TerminatedPfizer Inc.
VehicleJul 23, 2019
BMW lugs/nuts/bolts/studs recall — NHTSA campaign 19V541000
BMW of North America, LLC (BMW) is recalling certain 2019 X5 xDrive50i and X7 xDrive40i vehicles. The left side wheel bolts may have been insufficiently tightened and may loosen over time.
lugs/nuts/bolts/studsBMW of North America, LLC
Medical DeviceJul 17, 2019
Helena Laboratories ColoCARE, Cat. No. 5650, packaged 250 envelopes/box, For In-Vitro recall — FDA Z-1949-2019
The positive control on some tests of the lots did not appropriately react within the specified timeframe to verify the test was functioning correctly.
Class IIFDA: OngoingHelena Laboratories, Corp.
Medical DeviceJul 17, 2019
Richard Wolf Medical Instruments E-Line Cutting Electrode 11.5Fr Mono 0 degrees, Sterile recall — FDA Z-1957-2019
E-Line Cutting Electrode package 8416.0305 contains E-Line Hook Electrode 8416.09 instead of E-Line Cutting Electrode 8416.03.
Class IIFDA: TerminatedRichard Wolf Medical Instruments Corp.
Medical DeviceJul 17, 2019
Applied Medical Resources Kii Fios First Entry, 5 X 75 mm, RX only, REF CFF05 Qty: 6 recall — FDA Z-1959-2019
The product may not have met sterility requirements . Use of a non-sterile device on a patient may expose the patient to infectious agents.
Class IIFDA: TerminatedApplied Medical Resources Corp
Medical DeviceJul 17, 2019
Helena Laboratories ColoCARE, Cat. No. 5651, packaged 50 envelopes/box, For In-Vitro recall — FDA Z-1950-2019
The positive control on some tests of the lots did not appropriately react within the specified timeframe to verify the test was functioning correctly.
Class IIFDA: OngoingHelena Laboratories, Corp.
Medical DeviceJul 17, 2019
GE Healthcare Giraffe Infant Radiant Warmer Infant radiant warmers provide infrared heat in recall — FDA Z-1846-2019
The bedside panels and latch areas on the Giraffe Bedded Warmer and Panda iRes Warmer can crack or break if the unit is moved using the bedside panels instead of the front handle or the…
Class IFDA: TerminatedGE Healthcare, LLC
Medical DeviceJul 17, 2019
GE Healthcare Panda Infant Radiant Warmer Infant radiant warmers provide infrared heat in a recall — FDA Z-1847-2019
The bedside panels and latch areas on the Giraffe Bedded Warmer and Panda iRes Warmer can crack or break if the unit is moved using the bedside panels instead of the front handle or the…
Class IFDA: TerminatedGE Healthcare, LLC
Medical DeviceJul 17, 2019
Becton Dickinson & Company Alaris Pump Infusion Set, Model Codes 10010453, 10010454 recall — FDA Z-1770-2019
An incomplete occlusion can be caused by a variation in the wall thickness of the pumping segment of the affected infusion sets used with the. The issue has the potential to lead to…
Class IFDA: TerminatedBecton Dickinson & Company
Medical DeviceJul 17, 2019
Hamilton Medical AG HAMILTON-G5, with software versions less than or equal to 2.60 The recall — FDA Z-1874-2019
New software version for affected ventilators reduces the probability of the ventilator entering an ambient state, in which the inspiratory channel and expiratory valves are opened, letting…
Class IFDA: TerminatedHamilton Medical AG
Medical DeviceJul 17, 2019
COVIDIEN MAHURKAR and Argyle acute hemodialysis catheters, Material numbers 8813793009 recall — FDA Z-1955-2019
The priming volume values printed on the MAHURKA and Argyle acute catheters and Instructions for Use (IFU) are higher than the volumes required to fill each lumen.
Class IIFDA: TerminatedCOVIDIEN LLC
Medical DeviceJul 17, 2019
Rinovum Women's Health Revive Reusable Bladder Support, Model No. 0025 - Product Usage: The recall — FDA Z-1952-2019
The product is unable to meet the use life of 31 cycles and may split or crack at the base of the "petals" after repeated use but within the use life of the product (31 uses).
Class IIFDA: TerminatedRinovum Women's Health
Medical DeviceJul 17, 2019
Canon Medical System, USA Radrex-i X-Ray System (DRAD-3000E) TFP-4336W (Wireless FPD) recall — FDA Z-1958-2019
software malfunction; It was found when a user performs radiography using the wireless flat panel detector (FPD), a message window displays on the monitor stating image transmission was not…
Class IIFDA: TerminatedCanon Medical System, USA, 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.