FoodNov 15, 2017
Mann Packing Company 35.5 oz tray recall — FDA F-0176-2018
CFIA sampled one salad product which resulted in a positive result for Listeria monocytogenes.
Class IFDA: TerminatedMann Packing Company, Inc.
Latest records
Latest recalls — page 1549
The newest recall records with useful source details are listed here.
FoodNov 15, 2017
Mann Packing Company 16.5 oz trays recall — FDA F-0188-2018
CFIA sampled one salad product which resulted in a positive result for Listeria monocytogenes.
Class IFDA: TerminatedMann Packing Company, Inc.
FoodNov 15, 2017
Albertsons Broccoli/Cauliflower, 14 oz recall — FDA F-0229-2018
Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.
Class IFDA: TerminatedAlbertsons Inc.
FoodNov 15, 2017
San Gennaro Foods Red & Black Quinoa Organic Polenta, Ancient Harvest brand recall — FDA F-0125-2018
Date coding ink was being printed directly on the food contact surface of packaging, allowing the ink to be in direct contact with the product. The ink is not approved for food use.
Class IIIFDA: TerminatedSan Gennaro Foods, Inc.
FoodNov 15, 2017
San Gennaro Foods Sun-Dried Tomato Polenta, Melissa's brand, Shelf stable, 12/16 recall — FDA F-0117-2018
Date coding ink was being printed directly on the food contact surface of packaging, allowing the ink to be in direct contact with the product. The ink is not approved for food use.
Class IIIFDA: TerminatedSan Gennaro Foods, Inc.
FoodNov 15, 2017
Giant Eagle Market District Coffee Beans covered in Dark Chocolate recall — FDA F-0353-2018
On 10/30/2017, Giant Eagle received notice from their contract manufacturer to recall Market District Coffee Beans Covered in Dark Chocolate due to undeclared milk in the dark chocolate.…
Class IIFDA: TerminatedGiant Eagle, Inc.
FoodNov 15, 2017
Mann Packing Company 20.3 oz Tray recall — FDA F-0177-2018
CFIA sampled one salad product which resulted in a positive result for Listeria monocytogenes.
Class IFDA: TerminatedMann Packing Company, Inc.
FoodNov 15, 2017
San Gennaro Foods Traditional Polenta, San Gennaro brand, Pre-cooked Ready to recall — FDA F-0127-2018
Date coding ink was being printed directly on the food contact surface of packaging, allowing the ink to be in direct contact with the product. The ink is not approved for food use.
Class IIIFDA: TerminatedSan Gennaro Foods, Inc.
FoodNov 15, 2017
Mann Packing Company 16 oz bags - UPC 716519012174- US 12 oz bags - UPC recall — FDA F-0168-2018
CFIA sampled one salad product which resulted in a positive result for Listeria monocytogenes.
Class IFDA: TerminatedMann Packing Company, Inc.
DrugNov 15, 2017
Betadine Solution Swabstick Povidone-Iodine Solution USP, 10% Dist.by: Purdue Products LP recall — FDA D-0070-2018
Subpotent Drug: The laminate used to make the pouches was reversed such that the aluminum layer was in contact with the product causing an exothermic reaction between the free iodine and…
Class IIFDA: TerminatedPurdue Pharma, LP
DrugNov 15, 2017
Ace Surgical Supply Co Succinylcholine 20 MG/ML INJ (QUELICIN), 10 ML Vials recall — FDA D-0071-2018
Labeling: Incorrect or Missing Lot and/or Exp Date; incorrect expiration date on the labeling of the outer poly bag
Class IIFDA: TerminatedAce Surgical Supply Co., Inc.
DrugNov 15, 2017
Dr. Reddy's Laboratories Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol recall — FDA D-0072-2018
Labeling: Incorrect or Missing Lot and/or Exp Date; lot number on the secondary packaging doesnt match the lot number printed on the bottle
Class IIIFDA: TerminatedDr. Reddy's Laboratories, Inc.
Medical DeviceNov 8, 2017
Biosense Webster THERMOCOOL SMARTTOUCH Bi-Directional Navigation Catheter recall — FDA Z-0056-2018
Biosense Webster, Inc. has recently received an increased number of complaints related to the display of Alert 402 on the CARTO 3 System for certain lots of THERMOCOOL brand catheters.…
Class IIFDA: TerminatedBiosense Webster, Inc.
Medical DeviceNov 8, 2017
Biosense Webster THERMOCOOL SMARTTOUCH SF Bi-Directional Product Codes D-1348-01-S recall — FDA Z-0055-2018
Biosense Webster, Inc. has recently received an increased number of complaints related to the display of Alert 402 on the CARTO 3 System for certain lots of THERMOCOOL brand catheters.…
Class IIFDA: TerminatedBiosense Webster, Inc.
Medical DeviceNov 8, 2017
Teleflex Medical Teleflex(R) Percuvance(TM) Percutaneous Surgical System, Components: (a) 5 recall — FDA Z-0059-2018
Teleflex is recalling these products because the jaws of the tool tip may break, causing a fragment of the tool tip to fall off during use.
Class IIFDA: TerminatedTeleflex Medical
Medical DeviceNov 8, 2017
Biosense Webster THERMOCOOL SMARTTOUCH Uni-Directional Navigation Catheter (D133602S) recall — FDA Z-0057-2018
Biosense Webster, Inc. has recently received an increased number of complaints related to the display of Alert 402 on the CARTO 3 System for certain lots of THERMOCOOL brand catheters.…
Class IIFDA: TerminatedBiosense Webster, Inc.
Medical DeviceNov 8, 2017
Smiths Medical ASD CADD(TM) Yellow Medication Cassette Reservoir with clamp and female Luer recall — FDA Z-0062-2018
Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication Cassette Reservoirs may have been manufactured with an incorrect pressure plate.
Class IIFDA: TerminatedSmiths Medical ASD Inc.
Medical DeviceNov 8, 2017
Smiths Medical ASD CADD(TM) Medication Cassette Reservoir with clamp and female Luer recall — FDA Z-0060-2018
Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication Cassette Reservoirs may have been manufactured with an incorrect pressure plate.
Class IIFDA: TerminatedSmiths Medical ASD Inc.
Medical DeviceNov 8, 2017
Bios S.r.l THERMI250 Radiofrequency System recall — FDA Z-0052-2018
In some systems, the unit continues to emit RF energy after the PAUSE button is pressed.
Class IIFDA: TerminatedBios S.r.l.
Medical DeviceNov 8, 2017
Alcon Custom Pak recall — FDA Z-0053-2018
Alcon is initiating a medical device recall, after receiving notification from a supplier of a recall for x-ray detectable sponges. The one product referenced in the supplier recall…
Class IIFDA: TerminatedAlcon Research, LTD.
Medical DeviceNov 8, 2017
Biosense Webster THERMOCOOL SMARTTOUCH SF Uni-Directional Product Codes D-1347-01-S recall — FDA Z-0054-2018
Biosense Webster, Inc. has recently received an increased number of complaints related to the display of Alert 402 on the CARTO 3 System for certain lots of THERMOCOOL brand catheters.…
Class IIFDA: TerminatedBiosense Webster, Inc.
Medical DeviceNov 8, 2017
Smiths Medical ASD CADD(TM) Medication Cassette Reservoir with clamp and female Luer. recall — FDA Z-0061-2018
Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication Cassette Reservoirs may have been manufactured with an incorrect pressure plate.
Class IIFDA: TerminatedSmiths Medical ASD Inc.
Medical DeviceNov 8, 2017
Biosense Webster THERMOCOOL SF NAV Catheters Model Numbers - BNI35FJCT, BNI35DFCT recall — FDA Z-0058-2018
Biosense Webster, Inc. has recently received an increased number of complaints related to the display of Alert 402 on the CARTO 3 System for certain lots of THERMOCOOL brand catheters.…
Class IIFDA: TerminatedBiosense Webster, Inc.
FoodNov 8, 2017
Midway Specialty Vehicles Frosted Brownie Cookie, 96 1.5 oz recall — FDA F-0149-2018
Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily recalling multiple varieties of cookies sold between January 1, 2017 and September 28, 2017, because they may contain…
Class IIFDA: TerminatedMidway Specialty Vehicles LLC
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