FoodApr 11, 2018
Natural Grocers by Vitamin Cottage 10 oz recall — FDA F-0993-2018
Coconut smiles product tested positive for Salmonella.
Class IFDA: TerminatedNatural Grocers by Vitamin Cottage
Latest records
Latest recalls — page 1465
The newest recall records with useful source details are listed here.
FoodApr 11, 2018
Josie's Homestyle #1 Pralines Net Wt recall — FDA F-0985-2018
During an FDA inspection the firm was notified that the product was mislabeled due to the label indicating that the product contains cream when the firm actually uses evaporated milk and…
Class IIFDA: TerminatedJosie's Homestyle Pralines Etc. Inc.
FoodApr 11, 2018
Ventura Foods Gordon Choice Asian Sesame Ginger Dressing, Net recall — FDA F-0988-2018
A blue plastic bag was inadvertently introduced into product stream. During the manufacturing process, the blue plastic bag was torn into many pieces and ended up in the finished product.…
Class IIFDA: TerminatedVentura Foods, LLC
FoodApr 11, 2018
International Harvest Coconut Smiles - Retail: International Harvest Brand Organic recall — FDA F-0989-2018
Product tested positive for Salmonella.
Class IFDA: TerminatedInternational Harvest, Inc.
FoodApr 11, 2018
Tamarack ECLIPSE Kratom Premium Maeng Da, 40 count capsules and 2 oz recall — FDA F-0992-2018
Tamarack Inc. is recalling Eclipse Kratom-containing powder products because it may be contaminated with Salmonella.
Class IFDA: TerminatedTamarack, Inc.
FoodApr 11, 2018
The King Arthur Flour Company King Arthur Flour, 100% Organic, Finely Ground, Coconut Flour recall — FDA F-0991-2018
Coconut flour tested positive for Salmonella.
Class IFDA: TerminatedThe King Arthur Flour Company, Inc.
DrugApr 11, 2018
buPROPion HCl Extended-Release Tablets, USP (SR), 100 mg, 60 count bottles recall — FDA D-0618-2018
Failed Dissolution Specifications; during stability testing
Class IIIFDA: TerminatedInvaGen Pharmaceuticals, Inc.
DrugApr 11, 2018
buPROPion HCl Extended-Release Tablets, USP (SR), 150 mg ,a) 60 count (NDC 69097-878-03) and recall — FDA D-0619-2018
Failed Dissolution Specifications; during stability testing
Class IIIFDA: TerminatedInvaGen Pharmaceuticals, Inc.
Medical DeviceApr 4, 2018
ConMed MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Philips Plug Style Connector recall — FDA Z-1175-2018
Wire sets of certain devices were assembled with adhesive on the contact wires, which may impede conductivity and could cause failure
Class IIFDA: TerminatedConMed Corporation
Medical DeviceApr 4, 2018
Zimmer Biomet ACE Trochanteric Nail System TROCH NAIL ST 11X180 125DG STRL TROCH NAIL ST recall — FDA Z-1229-2018
Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to…
Class IIFDA: TerminatedZimmer Biomet, Inc.
Medical DeviceApr 4, 2018
Encore Medical Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 42mm, REF recall — FDA Z-1257-2018
It was discovered during a surgery that the design of the radius at the base of the pegs of the Anatomic Glenoid Trial (Part Numbers: 804-07-380, 804-07-420, 804-07-460, 804-07-500, and…
Class IIFDA: CompletedEncore Medical, Lp
Medical DeviceApr 4, 2018
St. Jude Medical Proclaim DRG Implantable Pulse Generator, Model Number 3664 recall — FDA Z-1170-2018
The firm received complaints of error messages that occurred during routine impedance checks on Proclaim DRG IPGs, model 3664. Some complaints were also associated with transient over…
Class IIFDA: TerminatedSt. Jude Medical, Inc.
Medical DeviceApr 4, 2018
Inova Diagnostics QUANTA-Lyser 240 IFA, Part #GS0242 recall — FDA Z-1221-2018
The device power supply was not manufactured according to specification which can result in the loss of the protective grounding of the instrument.
Class IIFDA: TerminatedInova Diagnostics Inc.
Medical DeviceApr 4, 2018
Roche Diagnostics Modular E 170 Analyzer: Immunoassay Chemistry Analyzer, Chemistry recall — FDA Z-1269-2018
Complaints have been received concerning questionable results on analyzers due to customers utilizing sample 13 mm tubes without tube adapters.
Class IIFDA: TerminatedRoche Diagnostics Corporation
Medical DeviceApr 4, 2018
Roche Diagnostics cobas e 411 Immunoassay Analyzer recall — FDA Z-1270-2018
Complaints have been received concerning questionable results on analyzers due to customers utilizing 13 mm sample tubes without tube adapters.
Class IIFDA: TerminatedRoche Diagnostics Corporation
Medical DeviceApr 4, 2018
Konica Minolta Medical Imaging USA Sonimage HS1 Ultrasound Kit AC adapter, Product Number recall — FDA Z-1212-2018
There is a risk of circuit board breakage within the main housing of the AC Adapter unit. Smoke may be emitted from the AC Adapter as a direct result.
Class IIFDA: TerminatedKonica Minolta Medical Imaging USA, Inc.
Medical DeviceApr 4, 2018
Johnson & Johnson BAND-AID Brand First Aid Products SECURE-FLEX Wrap (size: 3in) recall — FDA Z-1204-2018
Johnson & Johnson Consumer Inc. is initiating a voluntary, Class II recall at the retail level in the U.S. of select COACH Self-Adhering Sports Wraps, BAND-AID Brand First Aid Products…
Class IIFDA: TerminatedJohnson & Johnson Consumer, Inc.
Medical DeviceApr 4, 2018
Zimmer Biomet ACE Trochanteric Nail System ATN AR SCREW 60MM STERILE ATN AR SCREW 65MM recall — FDA Z-1233-2018
Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to…
Class IIFDA: TerminatedZimmer Biomet, Inc.
Medical DeviceApr 4, 2018
Konica Minolta Medical Imaging USA Sonimage HS1 Ultrasound Kit AC adapter, Product Number recall — FDA Z-1213-2018
There is a risk of circuit board breakage within the main housing of the AC Adapter unit. Smoke may be emitted from the AC Adapter as a direct result.
Class IIFDA: TerminatedKonica Minolta Medical Imaging USA, Inc.
Medical DeviceApr 4, 2018
Stryker Instruments Div. of Stryker 180-Gram Cement Cartridge with Breakaway Femoral Nozzle recall — FDA Z-1244-2018
Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable rates.
Class IIFDA: TerminatedStryker Instruments Div. of Stryker Corporation
Medical DeviceApr 4, 2018
Encore Medical Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 38mm, REF recall — FDA Z-1256-2018
It was discovered during a surgery that the design of the radius at the base of the pegs of the Anatomic Glenoid Trial (Part Numbers: 804-07-380, 804-07-420, 804-07-460, 804-07-500, and…
Class IIFDA: CompletedEncore Medical, Lp
Medical DeviceApr 4, 2018
Zimmer Dental Tapered Screw-Vent MTX, Dental Implant, sterile recall — FDA Z-1190-2018
Two lots of the Tapered Screw-Vent Implants, with different outer thread diameters, were inadvertently commingled during the manufacturing process and may be mislabeled.
Class IIFDA: TerminatedZimmer Dental Inc.
Medical DeviceApr 4, 2018
Keystone Dental STAGE-1 RDS COC Abutment Plastic Sleeve, Non-Lock, Multi-Unit recall — FDA Z-1179-2018
A locking plastic abutment sleeve, used by dental technicians in dental laboratories to aid in the creation of the final restorative crown, was packed as a non-locking plastic abutment…
Class IIIFDA: TerminatedKeystone Dental Inc.
Medical DeviceApr 4, 2018
Stryker Instruments Div. of Stryker 1. InterPulse Handpiece with coaxial bone cleaning tip recall — FDA Z-1246-2018
Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable rates.
Class IIFDA: TerminatedStryker Instruments Div. of Stryker Corporation
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
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