Medical DeviceJul 10, 2019
Zimmer Biomet DVR Crosslock ePAK Depth Gauge, Model Number 212000003 Product Usage: These recall — FDA Z-1947-2019
There is a potential for weak seals of the sterile packaging.
Class IIFDA: TerminatedZimmer Biomet, Inc.
Latest records
Latest recalls — page 1219
The newest recall records with useful source details are listed here.
Medical DeviceJul 10, 2019
Siemens Healthcare Diagnostics ADVIA Chemistry Creatine Kinase (CK_L) reagent, Product Code recall — FDA Z-1913-2019
A steady upward trend in blank (u) absorbance was observed
Class IIFDA: TerminatedSiemens Healthcare Diagnostics, Inc.
Medical DeviceJul 10, 2019
Siemens Medical Solutions USA SOMATOM go.Now, Model No. 11061618 with syngo.CT software recall — FDA Z-1920-2019
The potential sporadic performance problems may cause scanning workflow interruptions and unexpected user notifications resulting in diagnostic delay or need for patient rescan.
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Medical DeviceJul 10, 2019
Zimmer Biomet DVR Crosslock ePAK Screw Driver, Model Number 212000002 Product Usage: These recall — FDA Z-1946-2019
There is a potential for weak seals of the sterile packaging.
Class IIFDA: TerminatedZimmer Biomet, Inc.
Medical DeviceJul 10, 2019
Baxter Healthcare REVACLEAR 400 Dialyzer, Product Code 114746L Revaclear 300 and Revaclear recall — FDA Z-1909-2019
There is a potential presence of ruptured dialyzer fibers which may lead to a blood leak during treatment.
Class IIFDA: TerminatedBaxter Healthcare Corporation
Medical DeviceJul 10, 2019
Siemens Medical Solutions USA SOMATOM go.Up (Model #11061610) with syngo.CT software recall — FDA Z-1915-2019
The potential sporadic performance problems may result in scanning workflow interruptions and unexpected user notifications. This may cause a delay in diagnosis or patient scans.
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
FoodJul 10, 2019
Woolery Enterprises Inc. dba Will's Fresh Foods Will's Fresh Foods Macaroni Salad, All recall — FDA F-1525-2019
Wheat is not declared as an ingredient or allergen.
Class IIFDA: TerminatedWoolery Enterprises Inc. dba Will's Fresh Foods
FoodJul 10, 2019
UNFI General Corporate WOODSTOCK ORGANIC GRILLED RED PEPPER, NET WT 10 recall — FDA F-1527-2019
Product tested positive for Listeria monocytogenes.
Class IIFDA: TerminatedUNFI General Corporate
FoodJul 10, 2019
Nature's Touch Frozen Foods Signature Select Avocado Chunks, 12 oz recall — FDA F-1528-2019
Washington State Department of Agriculture sampled and tested frozen avocado and found Listeria monocytogenes.
Class IFDA: TerminatedNature's Touch Frozen Foods (West)
FoodJul 10, 2019
Tate & Lyle Ingredients Americas Food starch, brand names Miraqk Mgl and Nustar 120 and recall — FDA F-1526-2019
Product may contain small pieces of the wire due to a screen failure.
Class IIIFDA: TerminatedTate & Lyle Ingredients Americas, LLC
FoodJul 10, 2019
Ozark Country Kitchen Sorghum, Mfg recall — FDA F-1588-2019
Product contains high level of nitrates. Public health officials in Iowa are investigating two cases of methemoglobinemia possibly associated with consumption of the product.
Class IIFDA: TerminatedOzark Country Kitchen
DrugJul 10, 2019
Testosterone Topical Solution 30mg of testosterone per pump actuation * each actuation recall — FDA D-1454-2019
Defective Container; actuator may improperly function and affect dose delivery.
Class IIIFDA: TerminatedInvaGen Pharmaceuticals, Inc.
DrugJul 10, 2019
PharMEDium Services Hydromorphone HCl in 0.9% sodium chloride, 0.5mg per mL, 1 mL in 3mL BD recall — FDA D-1488-2019
Incorrect Product Formulation; Firm's customer resource center (CRC) statement indicates that the product is sulfite free, however the product is produced with a raw material that contains…
Class IFDA: TerminatedPharMEDium Services, LLC
DrugJul 10, 2019
Amneal Pharmaceuticals Esterified Estrogens & Methyltestosterone Tablets, USP 0.625 mg/1.25 recall — FDA D-1438-2019
Subpotent Drug: Out of specification assay result in Esterified Estrogen and Methyltestosterone tablets.
Class IIIFDA: TerminatedAmneal Pharmaceuticals, Inc.
DrugJul 10, 2019
Amneal Pharmaceuticals Esterified Estrogens & Methyltestosterone Tablets, USP 1.25 mg/2.5 recall — FDA D-1439-2019
Subpotent Drug: Out of specification assay result in Esterified Estrogen and Methyltestosterone tablets.
Class IIIFDA: TerminatedAmneal Pharmaceuticals, Inc.
VehicleJul 10, 2019
Ascent driveshaft recall — NHTSA campaign 19V519000
Subaru of America, Inc. (Subaru) is recalling certain 2019 Ascent vehicles. The center support bolts for the driveshaft may loosen, possibly resulting in the front portion of the driveshaft…
driveshaftSubaru of America, Inc.
VehicleJul 5, 2019
Mazda3 head restraint recall — NHTSA campaign 19V514000
Mazda North American Operations (Mazda) is recalling certain 2019 Mazda3 vehicles. The seat cover material on both front seats may interfere with the head restraint lock release button,…
head restraintMazda North American Operations
Medical DeviceJul 3, 2019
Thermo Scientific General Purpose Dynamic Bath Precision 5 & 10L Dual GP Bath recall — FDA Z-1871-2019
Product may have been assembled incorrectly,the assembly error can cause the bath to malfunction and raise the temperature of the fluid in the reservoir above the temperature set point…
Class IIFDA: TerminatedThermo Fisher Scientific (Asheville) LLC
Medical DeviceJul 3, 2019
AtriCure EPi-Sense Guided Coagulation System with Visitrax, MOdel No recall — FDA Z-1887-2019
The sterile package seal for the Epi-Sense Guided Coagulation System may be compromised, and has a worst-case reasonable harm of infection if used.
Class IIFDA: TerminatedAtriCure, Inc.
Medical DeviceJul 3, 2019
Thermo Scientific General Purpose Dynamic Bath Precision 28L GP Bath recall — FDA Z-1872-2019
Product may have been assembled incorrectly,the assembly error can cause the bath to malfunction and raise the temperature of the fluid in the reservoir above the temperature set point…
Class IIFDA: TerminatedThermo Fisher Scientific (Asheville) LLC
Medical DeviceJul 3, 2019
Medtronic Hancock II T510 Bioprosthesis, Mitral, REF T510C27 - Product Usage: Replacement of recall — FDA Z-1883-2019
Fifteen affected devices were distributed worldwide, which were mislabeled with an incorrect size. In all cases, the actual surgical heart valves are larger than what was indicated on the…
Class IIFDA: TerminatedMedtronic Inc.
Medical DeviceJul 3, 2019
Thermo Scientific General Purpose Dynamic Bath Precision 20L GP Bath recall — FDA Z-1869-2019
Product may have been assembled incorrectly,the assembly error can cause the bath to malfunction and raise the temperature of the fluid in the reservoir above the temperature set point…
Class IIFDA: TerminatedThermo Fisher Scientific (Asheville) LLC
Medical DeviceJul 3, 2019
GE Healthcare ECG leadwire sets: REF/Catalog Number Description 2106389-001 ECG Leadwire recall — FDA Z-1876-2019
ECG trunk cables and leadwires may reduce the amount of energy reaching the patient during defibrillation, potentially limiting success of defibrillating the patients rhythm.
Class IIIFDA: TerminatedGE Healthcare, LLC
Medical DeviceJul 3, 2019
Thermo Scientific General Purpose Dynamic Bath Precision 2L-Shallow GP Bath recall — FDA Z-1870-2019
Product may have been assembled incorrectly,the assembly error can cause the bath to malfunction and raise the temperature of the fluid in the reservoir above the temperature set point…
Class IIFDA: TerminatedThermo Fisher Scientific (Asheville) LLC
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026182 records · 4 categoriesSeptember 2026363 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories