FoodAug 19, 2026
Taylor Farms de Mexico S. de R.L. de C.V MARKON LETTUCE CHOP 4/5# MARKON LETTUCE SHRED 1/4" recall — FDA H-1281-2026
Potential Cyclospora contamination.
Class IFDA: OngoingTaylor Farms de Mexico S. de R.L. de C.V.
Latest records
Latest recalls — page 17
The newest recall records with useful source details are listed here.
FoodAug 19, 2026
Taylor Farms de Mexico S. de R.L. de C.V Cross Valley Farms LETTUCE SALAD MIX 4/5# Cross recall — FDA H-1292-2026
Potential Cyclospora contamination.
Class IFDA: OngoingTaylor Farms de Mexico S. de R.L. de C.V.
FoodAug 19, 2026
TAYLOR FARMS BLEND GARDEN SALAD MIX W/ROM 6/5# NATIONAL TAYLOR recall — FDA H-1291-2026
Potential Cyclospora contamination.
Class IFDA: OngoingTaylor Farms de Mexico S. de R.L. de C.V.
FoodAug 19, 2026
Taylor Farms de Mexico S. de R.L. de C.V MARKON BLEND LETT/ROM 50/50 NOCLR 4/5# MARKON BLEND recall — FDA H-1289-2026
Potential Cyclospora contamination.
Class IFDA: OngoingTaylor Farms de Mexico S. de R.L. de C.V.
FoodAug 19, 2026
Taylor Farms de Mexico S. de R.L. de C.V Romaine, Carrots, Red Cabbage products recall — FDA H-1299-2026
Potential Cyclospora contamination.
Class IFDA: OngoingTaylor Farms de Mexico S. de R.L. de C.V.
FoodAug 19, 2026
Lyle Style 32oz recall — FDA 99517
Undeclared Soy. Finished product ingredients statement declares Worcestershire sauce but does not declare sub-ingredients Soy Flavoring and Soy Lecithin.
Class IIFDA: TerminatedLyle Style
FoodAug 19, 2026
Taylor Farms de Mexico S. de R.L. de C.V Cross Valley Farms BLEND LETT/ROM 80/20 WITH SEP recall — FDA H-1297-2026
Potential Cyclospora contamination.
Class IFDA: OngoingTaylor Farms de Mexico S. de R.L. de C.V.
FoodAug 19, 2026
Taylor Farms de Mexico S. de R.L. de C.V MARKON LETTUCE SALAD MIX 4/5# MARKON LETTUCE SALAD recall — FDA H-1293-2026
Potential Cyclospora contamination.
Class IFDA: OngoingTaylor Farms de Mexico S. de R.L. de C.V.
Medical DeviceAug 19, 2026
Philips Azurion Rystem, Model Numbers: 722063, 722064, 722067, 722068, 722078, 722079 recall — FDA Z-2931-2026
Two software related issues affecting Azurion R2.2.10 Systems: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropriate…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceAug 19, 2026
BIOFIRE Respiratory Panel 2.1 (RP2.1) REF 423742 UDI code: 00815381020529 PCR-based recall — FDA Z-2936-2026
Due to increase in false negative results
Class IIFDA: OngoingBioFire Diagnostics, LLC
Medical DeviceAug 19, 2026
OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF recall — FDA Z-2933-2026
There is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions for both the patient and the healthcare…
Class IIFDA: OngoingOBP Medical Corporation
Medical DeviceAug 19, 2026
Covidien Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31 DERMALON* recall — FDA Z-2920-2026
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of vision if…
Class IIFDA: OngoingCovidien, LP
Medical DeviceAug 19, 2026
Cardinal Health Presource Kits: 1) BASIC PACK recall — FDA Z-2949-2026
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceAug 19, 2026
Covidien Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623 recall — FDA Z-2921-2026
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of vision if…
Class IIFDA: OngoingCovidien, LP
Medical DeviceAug 19, 2026
Bioporto Diagnostics A/S ProNephro AKI (NGAL) Reagent Kit (100 tests) recall — FDA Z-2937-2026
The use of a non-validated rework process for assay reagents which could lead to missed diagnosis of renal disease, inappropriate treatment decisions, or inappropriate monitoring of renal…
Class IIFDA: OngoingBioporto Diagnostics A/S
Medical DeviceAug 19, 2026
Straumann USA GM Helix Implant, Endosseous Dental Implant Article No. 109.984 recall — FDA Z-2929-2026
There may be a mismatch between the implant contained inside the packaging and the information described on the outer carton label. If the the incorrect implant is installed, the issue…
Class IIFDA: OngoingStraumann USA LLC
Medical DeviceAug 19, 2026
Cardinal Health Presource Kits: 1) SEPTO RHINO PACK recall — FDA Z-2946-2026
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceAug 19, 2026
Waldemar Link GmbH & Co. KG Endo-Model, Replacement Set, Tibial Plateau, right/left, L recall — FDA Z-2934-2026
The affected Endo-Model replacement set for a Rotating Hinge tibial plateau incorrectly contains a Pure Hinge plateau. The incorrect plateau could lead to a prolonged or modified surgery as…
Class IIFDA: OngoingWaldemar Link GmbH & Co. KG (Mfg Site)
Medical DeviceAug 19, 2026
BD SWITZERLAND SARL 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code recall — FDA Z-2941-2026
Products may not have received adequate sterilization processing.
Class IIFDA: OngoingBD SWITZERLAND SARL
Medical DeviceAug 19, 2026
Xhibit Central Station recall — FDA Z-2916-2026
Due to off-the-shelf display port component that has audio/video failures
Class IIFDA: OngoingSpacelabs Healthcare, Inc.
Medical DeviceAug 19, 2026
W L Gore & Associates GORE VIABIL Short Wire Biliary Endoprosthesis, Model No recall — FDA Z-2915-2026
10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes (VSWVN1010).
Class IIFDA: OngoingW L Gore & Associates, Inc.
Medical DeviceAug 19, 2026
Straumann Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim recall — FDA Z-2935-2026
Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim may inadvertently contain implants that are 12mm in length instead of 14mm as the labeling would suggest.
Class IIFDA: OngoingStraumann USA LLC
Medical DeviceAug 19, 2026
Covidien V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 VLOC 90 0 recall — FDA Z-2918-2026
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of vision if…
Class IIFDA: OngoingCovidien, LP
Medical DeviceAug 19, 2026
Erbe USA ERBECRYO 2 Cryosurgical Unit recall — FDA Z-2938-2026
A strong pull on the high-pressure transfer hose of cryosurgical unit may lead to pneumatic short circuit between he gas inlet and the connector resulting in CO2 leaking into the return…
Class IIFDA: OngoingErbe USA Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 2026300 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 categoriesOctober 2025455 records · 4 categories