FoodJul 29, 2026
Shandong Ling Xian Food Co NAUTILUS IMITATION CRAB STICKS NET WT: 1.0 LB recall — FDA H-1183-2026
Undeclared sodium tripolyphosphate (STTP)
Class IIIFDA: OngoingShandong Ling Xian Food Co.,LTD
Monthly breakdown
2026 recalls by month
Select a month to review the recall records reported during that period.
August 2026144 records · 4 categoriesJuly 2026363 records · 4 categoriesJune 2026368 records · 4 categoriesMay 2026327 records · 4 categoriesApril 2026405 records · 4 categoriesMarch 2026170 records · 3 categoriesFebruary 2026120 records · 4 categoriesJanuary 202661 records · 3 categories
2026 recalls — page 10
Records are ordered by the best available source date.
FoodJul 29, 2026
Shandong Ling Xian Food Co Island Pacific IMITATION CRAB STICKS NET WT: 1.0 LB recall — FDA H-1182-2026
Undeclared sodium tripolyphosphate (STTP)
Class IIIFDA: OngoingShandong Ling Xian Food Co.,LTD
FoodJul 29, 2026
Shandong Ling Xian Food Co Island Pacific IMITATION CRAB FLAKES NET WT: 1.0 LB recall — FDA H-1184-2026
Undeclared sodium tripolyphosphate (STTP)
Class IIIFDA: OngoingShandong Ling Xian Food Co.,LTD
FoodJul 29, 2026
Vintage Roots packaged in glass bottle recall — FDA H-1177-2026
Unapproved food additive: sassafras bark.
Class IIFDA: TerminatedVintage Roots LLC
FoodJul 29, 2026
Man Fon Wonton Wrappers packed into clear flexible plastic bag and recall — FDA H-1188-2026
No labeling. Undeclared wheat and colors: Yellow#5, Yellow#6.
Class IIFDA: OngoingMan Fon, Inc.
FoodJul 29, 2026
Man Fon Inc recall — FDA H-1187-2026
Undeclared colors: Yellow#5, and Yellow#6.
Class IIFDA: OngoingMan Fon, Inc.
FoodJul 29, 2026
Brooklyn Roasting Company Pasteurized Cold Brew Concentrate recall — FDA H-1179-2026
Ambient storage of the product may lead to Clostridium botulinum toxin formation.
Class IIFDA: CompletedBrooklyn Roasting Works LLC
VehicleJul 28, 2026
Ford display function recall — NHTSA campaign 26V489000
Ford Motor Company (Ford) is recalling certain 2021-2023 F-150 and 2023-2026 F-250 SD vehicles equipped with 8-inch SYNC infotainment screens. A software error may cause the rearview camera…
display functionFord Motor Company
Medical DeviceJul 22, 2026
ABIOMED Introducer Kit 23 Fr, 11 cm, Pump Set Code 1000441, containing Kit, 23Fr Introducer recall — FDA Z-2684-2026
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually…
Class IFDA: OngoingAbiomed, Inc.
Medical DeviceJul 22, 2026
ABIOMED Impella CP Smart Assist Set, JP, Pump Set Code 0048-0024-JP recall — FDA Z-2690-2026
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually…
Class IFDA: OngoingAbiomed, Inc.
Medical DeviceJul 22, 2026
ABIOMED Intro Kit, 14Fr x 13 and 25 cm, PKGD, JP, Pump Set Code 0052-0023-JP recall — FDA Z-2693-2026
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually…
Class IFDA: OngoingAbiomed, Inc.
Medical DeviceJul 22, 2026
ABIOMED Impella 5.5 Smart Assist Set, JP, Pump Set Codes 1000211, 1000212 recall — FDA Z-2687-2026
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually…
Class IFDA: OngoingAbiomed, Inc.
Medical DeviceJul 22, 2026
Oscor Abiomed REF: 0052-3006, Introducer Kit for Impella Hemostatic Peel Away Introducer recall — FDA Z-2680-2026
Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub region.
Class IFDA: OngoingOscor Inc.
Medical DeviceJul 22, 2026
ABIOMED Impella CP Set, Pump Set Code 0048-0044 recall — FDA Z-2691-2026
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually…
Class IFDA: OngoingAbiomed, Inc.
Medical DeviceJul 22, 2026
Rio" II Nasal Pillows Interface recall — FDA Z-2740-2026
Packaging and labeling discrepancy involving product size identification and associated Unique Device Identifier (UDI/GTIN).
Class IIFDA: Ongoing3B Medical, Inc.
Medical DeviceJul 22, 2026
ABIOMED Impella RP Flex with SmartAssist Set, Pump Set Code 1000323, containing Kit, 23Fr recall — FDA Z-2681-2026
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually…
Class IFDA: OngoingAbiomed, Inc.
Medical DeviceJul 22, 2026
Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010 recall — FDA Z-2738-2026
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
Class IIFDA: OngoingMedtronic Perfusion Systems
Medical DeviceJul 22, 2026
Intuitive Surgical da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13 recall — FDA Z-2722-2026
Robotic-assisted surgical system arm drapes may detach from the instrument arm due to an issue involving the drape rings located at the top of the product, which may expose a section of…
Class IIFDA: OngoingIntuitive Surgical, Inc.
Medical DeviceJul 22, 2026
Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK-LF recall — FDA Z-2737-2026
Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach. Health consequences from use of product include…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJul 22, 2026
Olympus Toomey Evacuator 50cc with Adaptor recall — FDA Z-2719-2026
Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to sterilize the devices.
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceJul 22, 2026
Orthofix MINIRAIL, SHORT, LENGTHENER REF: M103, Unilateral orthopedic/trauma external recall — FDA Z-2730-2026
Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111
Class IIFDA: OngoingOrthofix U.S. LLC
Medical DeviceJul 22, 2026
GE Medical Systems Optima XR240amx, Mobile Digital Radiographic System recall — FDA Z-2728-2026
GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety pawl may not have been…
Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceJul 22, 2026
Maquet Cardiovascular The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System recall — FDA Z-2741-2026
Getinge identified that Vasoview Hemopro 2 devices from Lot 3000547797 were exposed to an out-of-specification sterilization dose during a gamma sterilization run (Run ID 1183-28782A)…
Class IIFDA: OngoingMaquet Cardiovascular, LLC
Medical DeviceJul 22, 2026
ABIOMED Impella 5.5 SmartAssist S2 Set, JP, Pump Set Codes 1000459, 1000460 recall — FDA Z-2688-2026
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually…
Class IFDA: OngoingAbiomed, Inc.
About the 2026 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.