Medical DeviceMar 11, 2026
B. Braun 21GA WINGED INFUSION, SINGLE PK recall — FDA Z-1482-2026
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
Class IIFDA: OngoingB Braun Medical Inc
Monthly breakdown
2026 recalls by month
Select a month to review the recall records reported during that period.
August 2026145 records · 4 categoriesJuly 2026369 records · 4 categoriesJune 2026373 records · 4 categoriesMay 2026330 records · 4 categoriesApril 2026407 records · 4 categoriesMarch 2026179 records · 4 categoriesFebruary 2026329 records · 4 categoriesJanuary 2026210 records · 4 categories
2026 recalls — page 73
Records are ordered by the best available source date.
Medical DeviceMar 11, 2026
Datascope CS100 IABP. Software Version CS100 IABP Q.01 recall — FDA Z-1486-2026
The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.
Class IIFDA: OngoingDatascope Corp.
Medical DeviceMar 11, 2026
Siemens Healthcare Diagnostics Atellica CH Urine Albumin (UAlb) recall — FDA Z-1484-2026
Falsely depressed UAlb patient results may occur. Affected samples with any urine albumin concentration above the UAlb measuring interval >40.0 mg/dL may report values between 6.2 mg/dL and…
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceMar 11, 2026
Datascope CS300 IABP. Software Version CS300 IABP C.01 recall — FDA Z-1487-2026
The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.
Class IIFDA: OngoingDatascope Corp.
Medical DeviceMar 11, 2026
GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: 2110344-039 recall — FDA Z-1475-2026
Under certain workflows, patient information shown in the viewer may not match the images displayed on Centricity Universal Viewer Zero Footprint Client (ZFP) with versions ZFP v6.0:…
Class IIFDA: OngoingGE Healthcare
Medical DeviceMar 11, 2026
Roche Diagnostics Operations cobas pro integrated solutions with cobas c 503 analytical recall — FDA Z-1476-2026
Software defect, which allows the system to accept erroneous, non-monotonous calibrations for Spline-type assays. Cobas pro integrated solutions is an automated analyzer, intended for…
Class IIFDA: OngoingRoche Diagnostics Operations, Inc.
Medical DeviceMar 11, 2026
Esaote Endocavity ultrasonic probe, Model E 3-12, REF 120000038 recall — FDA Z-1490-2026
A potential weakness has been identified in the probe body, so that, in a specific production batch, liquid may leak from the terminal part of the casing near the cable.
Class IIFDA: CompletedESAOTE S.P.A.
Medical DeviceMar 11, 2026
AESCULAP MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM recall — FDA Z-1485-2026
There is the potential for the length of the trocar shaft to be too long.
Class IIFDA: OngoingAesculap Inc
Medical DeviceMar 11, 2026
Staar Surgical AG EVO+ Visian Toric Implantable Collamer Lens (TICL), Model: VTICM5 recall — FDA Z-1480-2026
Toric Implantable Collamer for correction/reduction of myopia in phakic eyes with astigmatism were labeled as 12.1 mm length but are 12.6 mm length lenses, so there is the potential for…
Class IIFDA: OngoingStaar Surgical AG
Medical DeviceMar 11, 2026
B. Braun 21GA WINGED INF SET recall — FDA Z-1483-2026
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
Class IIFDA: OngoingB Braun Medical Inc
Medical DeviceMar 11, 2026
ShockPulse-SE Lithotripsy System - Generator recall — FDA Z-1479-2026
Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the transducer plug and/or…
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceMar 11, 2026
Abiomed Impella RP with SmartAssist recall — FDA Z-1469-2026
Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.
Class IFDA: OngoingAbiomed, Inc.
Medical DeviceMar 11, 2026
Olympus Single Use Biopsy Valve recall — FDA Z-1489-2026
Potential for rubber fragment detachment during use.
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceMar 11, 2026
Abiomed Impella RP Flex with SmartAssist recall — FDA Z-1470-2026
Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.
Class IFDA: OngoingAbiomed, Inc.
Medical DeviceMar 11, 2026
Olympus Single use Biopsy Valve recall — FDA Z-1488-2026
Potential for rubber fragment detachment during use.
Class IIFDA: OngoingOlympus Corporation of the Americas
FoodMar 11, 2026
Bader Enterprises Premium Food Bubble Gum, packed in 2.5 oz clear flexible recall — FDA H-0539-2026
Contains undeclared colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake).
Class IIFDA: OngoingBader Enterprises, Inc.
FoodMar 11, 2026
Perfect Pasta Lobster & Crab Ravioli recall — FDA H-0620-2026
Undeclared shrimp, crab, lobster, pollock (fish), whiting (fish), and soy.
Class IFDA: TerminatedPerfect Pasta, Incorporated
FoodMar 11, 2026
Bader Enterprises Premium Food Jordan Almonds, packed in 2.0 oz and 3.5 oz clear recall — FDA H-0538-2026
Contains undeclared allergen (wheat) and colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake).
Class IIFDA: OngoingBader Enterprises, Inc.
FoodMar 11, 2026
Italianway Import VERGANI 1944 MILANO 'PANDORO CLASSICO' Gluten Free, 600g NET recall — FDA H-0540-2026
Potential contamination with foreign material (Teflon fragments) from flaking cooking molds.
Class IIFDA: TerminatedItalianway Import, Inc.
FoodMar 11, 2026
Juniper Granola Junebar Peanut Chocolate Chip All Natural Snack Bar recall — FDA H-0542-2026
Products contain undeclared milk and soy.
Class IFDA: TerminatedJuniper Granola, LLC
FoodMar 11, 2026
IF Holding II tippy toes apple pear banana 6 months & up baby food 2-4OZ recall — FDA H-0544-2026
Potential contamination with patulin.
Class IIFDA: OngoingIF Holding II, LLC
FoodMar 11, 2026
Juniper Granola Junebar Chocolate Cherry All Natural Snack Bar recall — FDA H-0543-2026
Products contain undeclared milk and soy.
Class IFDA: TerminatedJuniper Granola, LLC
DrugMar 11, 2026
ACME UNITED 1) BZK Antiseptic Towelettes recall — FDA D-0362-2026
CGMP Deviations
Class IIFDA: OngoingACME UNITED CORPORATION
DrugMar 11, 2026
Sodium Iodide (I-131) Solution, Therapeutic Oral, packaged as a) 1 ml V-vial, NDC recall — FDA D-0389-2026
Presence of Particulate Matter: Due to production issues
Class IIFDA: OngoingRadnostix
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.