Medical DeviceJun 1, 2022
TELEFLEX MEDICAL (1) Teleflex Flex tube, Product #20011, sterile recall — FDA Z-1127-2022
Reports received of torn corrugated breathing tubes.
Class IIFDA: OngoingTELEFLEX MEDICAL Inc.
Latest records
Latest recalls — page 726
The newest recall records with useful source details are listed here.
Medical DeviceJun 1, 2022
Accriva Diagnostics The VerifyNow P2Y12 Test is designed to measure platelet P2Y12 receptor recall — FDA Z-1121-2022
Two whole blood Platelet Reactivity tests exist that share the same reagent formulation and are used to obtain P2Y12 Reactivity Unit results. The test without US-FDA market clearance was…
Class IIFDA: TerminatedAccriva Diagnostics, Inc.
Medical DeviceJun 1, 2022
International Science & Technology, LP, DBA Outer Packaging Label: Protekt Sharps Safety recall — FDA Z-1120-2022
Surgical knives may contain incorrect description printed on handles. Specifically, some surgical knife handles may contain a size of "2.5mm" when the actual size is "2.2mm".
Class IIFDA: CompletedInternational Science & Technology, LP, DBA Diamatrix…
Medical DeviceJun 1, 2022
Smith & Nephew Orthopaedics GmbH INTERTAN 1.5 NAIL 13mm X 42cm 130DEG recall — FDA Z-1133-2022
Right nails were anodized, marked, and labelled as left nails and vice versa
Class IIFDA: OngoingSmith & Nephew Orthopaedics GmbH
Medical DeviceJun 1, 2022
Umano Medical AC-powered adjustable medical beds with built-in electric DC actuators and recall — FDA Z-1136-2022
There is a potential hazard of uninterrupted motion of the Motorized Wheel System due to the possible failure of a component in the electrical system of the Product.
Class IIFDA: TerminatedUmano Medical, Inc.
Medical DeviceJun 1, 2022
Medtronic Neuromodulation Percept BrainSense Implantable Neurostimulator (INS), Model B35200 recall — FDA Z-1128-2022
The Implantable Neurostimulator (INS) cannot communicate with the clinical programmer and/or the patient programmer system.
Class IIFDA: OngoingMedtronic Neuromodulation
Medical DeviceJun 1, 2022
Devicor Medical Products HydroMARK Breast Biopsy Marker, Model No. 4010-05-08-T4 recall — FDA Z-1124-2022
Small patient labels do not match the primary device label. The primary device label accurately identifies the product as 4010-05-08-T4, while the smaller patient label incorrectly…
Class IIFDA: TerminatedDevicor Medical Products Inc.
Medical DeviceJun 1, 2022
Invacare TDX SP2, Model Nos recall — FDA Z-1130-2022
The battery wiring harness on affected wheelchairs may become disconnected during shipment from the factory or during wheelchair use traversing large obstacles or after a jolt or impact to…
Class IIFDA: OngoingInvacare Corporation
Medical DeviceJun 1, 2022
Medtronic Neuromodulation Percept PC BrainSense Implantable Neurostimulator (INS) Model recall — FDA Z-1129-2022
The Implantable Neurostimulator (INS) cannot communicate with the clinical programmer and/or the patient programmer system.
Class IIFDA: OngoingMedtronic Neuromodulation
Medical DeviceJun 1, 2022
TELEFLEX MEDICAL (1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile recall — FDA Z-1126-2022
Reports received of torn corrugated breathing tubes.
Class IIFDA: OngoingTELEFLEX MEDICAL Inc.
Medical DeviceJun 1, 2022
Medtronic Perfusion Systems Cardioblate" Gemini"-s Irrigated RF Surgical Ablation System recall — FDA Z-1131-2022
Firm detected an increase in complaints related to fractured jaw tips of the Cardioblate Gemini-s.
Class IIFDA: OngoingMedtronic Perfusion Systems
Medical DeviceJun 1, 2022
Umano Medical AC-powered adjustable medical beds with built-in electric DC actuators and recall — FDA Z-1135-2022
There is a potential hazard of uninterrupted motion of the Motorized Wheel System due to the possible failure of a component in the electrical system of the Product.
Class IIFDA: TerminatedUmano Medical, Inc.
Medical DeviceJun 1, 2022
Medtronic Neuromodulation Vanta INS Implantable Neurostimulator recall — FDA Z-1123-2022
The Implantable Neurostimulator Model may be susceptible to not communicating with the clinical programmer and/or patient programmer system.
Class IIFDA: OngoingMedtronic Neuromodulation
Medical DeviceJun 1, 2022
ConvaTec SUR-FIT Natura S4S Durahesive Wafer 70MM (1X10PK) US recall — FDA Z-1134-2022
Firm received 10 complaints of skin barrier delamination issues (e.g. flange lifts from wafer, skin barrier layers separate) or tape border rips/tears.
Class IIFDA: TerminatedConvaTec, Inc.
Medical DeviceJun 1, 2022
ProgenaCare progenamatrix Human Keratin Matrix, sterile, Rx, with the following model recall — FDA Z-1137-2022
Inner pouch seal may be inadequate resulting in lack of sterility.
Class IIFDA: TerminatedProgenaCare
FoodJun 1, 2022
H-E-B Grocery Company, LP DBA HEB Milk & Culture HEB Bakery Simply Delicious Cookies with recall — FDA F-1084-2022
potential metal fragments in product
Class IIFDA: TerminatedH-E-B Grocery Company, LP DBA HEB Milk & Culture Plant…
FoodJun 1, 2022
Damascus Bakery Bantam Bagels Everybody's Favorite Everything Bagel Stuffed recall — FDA F-1087-2022
Product contains undeclared egg allergen.
Class IFDA: TerminatedDamascus Bakery LLC
FoodJun 1, 2022
Mrs Millers Homemade Jams LLC Mrs recall — FDA F-1089-2022
Undeclared Allergen - Soy
Class IIFDA: TerminatedMrs Millers Homemade Jams LLC.
FoodJun 1, 2022
Mrs Millers Homemade Jams LLC Mrs recall — FDA F-1088-2022
Undeclared Allergen - Soy
Class IIFDA: TerminatedMrs Millers Homemade Jams LLC.
FoodJun 1, 2022
Joonsung Trading Champon Soup Base packaged in 32 oz plastic jug recall — FDA F-1076-2022
Undeclared milk and tuna. Label declares Hondashi but does not declare Milk and Tuna.
Class IFDA: TerminatedJoonsung Trading Inc.
FoodJun 1, 2022
Joonsung Trading Spicy Chicken Sauce packaged in 1/2 gallon plastic jug recall — FDA F-1079-2022
Undeclared wheat. Label declares Hot Bean Paste but does not declared Wheat.
Class IFDA: TerminatedJoonsung Trading Inc.
FoodJun 1, 2022
Joonsung Trading Chirashi Sauce packaged in 1/2 gallon plastic jug recall — FDA F-1077-2022
Undeclared soy and wheat. Label declares Hot Bean Paste but does not declare Soy and Wheat.
Class IFDA: TerminatedJoonsung Trading Inc.
DrugJun 1, 2022
Preferred Pharmaceuticals Losartan Potassium & HCTZ Tablets 50mg/12.5 mg recall — FDA D-0892-2022
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Class IIFDA: TerminatedPreferred Pharmaceuticals, Inc.
DrugJun 1, 2022
Olympia Compounding Pharmacy dba Olympia Lipo-Mino-Mix Pyridoxine HCL (B6) 2 mg/mL recall — FDA D-0932-2022
Lack of assurance of sterility.
Class IIFDA: CompletedOlympia Compounding Pharmacy dba Olympia Pharmacy
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Recent recall archives
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October 2026110 records · 3 categoriesSeptember 2026364 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