Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

6951–6975 of 13666

HighFDA (Devices)·Z-1347-2024·2024-03-27
Vascular guidewire introducer recalled for manufacturing defect causing procedural delays
Angiodynamics recalls the MINI STICK MAX vascular guidewire introducer due to internal defects in the sheath hub that may prevent guidewire insertion during surgery, potentially requiring equipment exchange.
Product
MINI STICK MAX 5F X 15 CM STIFF .018 NI/TU NON-ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-776
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1337-2024·2024-03-27
Guidewire Introducer Recalled for Manufacturing Defect Affecting Device Function
Angiodynamics is recalling 58 units of its MINI STICK MAX guidewire introducer due to voids in the internal lumen that may prevent proper guidewire passage. Users may experience procedural delay requiring device exchange.
Product
MINI STICK MAX 4F X 10 CM STIFF .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-752
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1321-2024·2024-03-27
Preat Nobel RP Titanium Abutment Blank Recalled for Manufacturing Defect
Preat Corp is recalling 561 units of RP Titanium Abutment Blanks due to a manufacturing defect where the screw seat location may be too high, resulting in shortened screw engagement into the implant.
Product
Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1343-2024·2024-03-27
Vascular Guidewire Introducer Sheath Recalled for Internal Hub Defect
Angiodynamics recalls 130 MINI STICK MAX guidewire introducers due to hub voids that may prevent guidewire passage during vascular procedures. No injuries reported.
Product
MINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-765
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1348-2024·2024-03-27
Guidewire Introducer Sheath Recalled for Internal Lumen Voids
Angiodynamics is recalling 39 units of MINI STICK MAX vascular guidewire introducers due to voids in the sheath hub that may prevent guidewire passage during surgery, potentially delaying the procedure.
Product
MINI STICK MAX 4F X 10CM STIFF .018 NI/TU ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. - Catalog Number: 45-781
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1331-2024·2024-03-27
Directional Laser Probe Recalled for Fiber Extension and Direction Difficulties
D.O.R.C. Dutch Ophthalmic Research Center is recalling Directional Laser Probes for ophthalmic surgery due to difficulties extending, retracting, and directing the laser fiber. The recall affects 84 units distributed nationwide.
Product
Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1350-2024·2024-03-27
Convatec EsteemBody Drainable Pouches Recalled for Filter Weld Defect
ConvaTec is recalling specific lots of EsteemBody Soft Convex Drainable Pouches due to inconsistency in filter weld strength, affecting 6709 units distributed in the US and internationally.
Product
Convatec EsteemBody Soft Convex, Drainable Pouch, Product codes (REF): a) 423643, b) 423658, c) 423659, d) 423664, e) 423666, f) 423645, g) 423667, h) 423657, i) 423652, j) 423646, k) 423654, l) 423653, m) 423647, n) 423644, o) 423648, p) 423665, q) 423656, r) 423651, s) 423660,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1330-2024·2024-03-27
Laparotomy Sponges recalled for incomplete sterilization and missing RF detection
Covidien is recalling Situate Laparotomy Sponges because some packs may contain improperly sterilized units lacking required RF detection features. Non-sterile sponges could cause infection, tissue trauma, and sepsis during surgery.
Product
Situate Laparotomy Sponge, RF and X-ray Detectable, REF: L1818-04P01C-1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1341-2024·2024-03-27
Angiodynamics Guidewire Introducer Recall Due to Manufacturing Defect
Angiodynamics recalls approximately 5,840 guidewire introducers with manufacturing defects that may prevent proper guidewire insertion during vascular procedures. The defect could cause procedural delays requiring equipment exchange.
Product
MINI STICK MAX 5F X 10 CM STIFF .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-759
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1312-2024·2024-03-27
Pregnancy Test Control Set Recalled for Temperature Excursion Risk
McKesson recalls Abbott Rapid Dx pregnancy test control sets due to a refrigerator temperature excursion that could cause inaccurate or delayed test results.
Product
Abbott Rapid Dx N America LLC Reproductive Endocrinology Control Set McKesson Consult" Pregnancy (hCG) Testing Positive Level / Negative Level 2 X 4 mL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1320-2024·2024-03-27
Medical Device Recall: Orthopedic Compression Screws with Incorrect Dimensions
In2Bones, SAS is recalling I.B.S Compression screws due to a batch mix-up. Affected screws may have different lengths than indicated on their labels, creating a risk of improper surgical implantation.
Product
I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 80mm,Part Number S65 ST180
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1307-2024·2024-03-27
Nasal Intubation Kit Recalled for Incompatible Tube Holder
Curaplex Nasal Intubation Kit recalled because the included endotracheal tube holder is incompatible with nasal intubation procedures, preventing practitioners from properly securing the tube.
Product
Curaplex Nasal Intubation Kit with 6mm Endotrol Tube-To perform a nasal intubation to establish an airway in an emergency. Item Number: 023060S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1318-2024·2024-03-27
TMINI Knee Instrument Array Guide May Bind During Surgical Drilling
A precision component in Think Surgical's TMINI robotic knee system may bind due to insufficient clearance. The binding could occur during surgical drilling.
Product
Assembly, Array Guide TMINI, REF: 109101, part of the TMINI Knee Instrument Set, used with the TMINI Miniature Robotic System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1334-2024·2024-03-27
Vascular guidewire introducer recalled for manufacturing defect
Angiodynamics recalls MINI STICK MAX vascular guidewire introducers due to internal lumen defects that may prevent the guidewire from passing through during surgery, potentially requiring device exchange.
Product
MINI STICK MAX 4F X 10 CM STD .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-749
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1333-2024·2024-03-27
Directional Laser Probe Recalled for Fiber Extension and Direction Failure
D.O.R.C. recalls 78 directional laser probes with Alcon/Lumenis connectors due to difficulties extending, retracting, or directing the laser fiber. The Class II recall affects units distributed across multiple U.S. states and Puerto Rico.
Product
Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1338-2024·2024-03-27
Vascular Guidewire Introducer Sheath Recall Due to Manufacturing Defect
Angiodynamics is recalling certain MINI STICK MAX vascular guidewire introducer sheaths due to internal voids that may prevent guidewire passage during surgery, potentially causing procedural delays.
Product
MINI STICK MAX 5F X 10 CM STD .018 SS/SS ECHO 2.75" PG -Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-754
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1313-2024·2024-03-27
Steris Endo Cleaning Indicator Recalled Due to Temperature Excursion
Mckesson Medical-Surgical is recalling Steris Endo Cleaning Indicator VERIFY RESITEST devices due to temperature excursions that occurred on January 8, 2024. The temperature drop could cause the indicator to produce incorrect or delayed test results.
Product
Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST"
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1336-2024·2024-03-27
FDA Recalls Vascular Guidewire Introducer Due to Manufacturing Defect
Angiodynamics is recalling 959 units of MINI STICK MAX guidewire introducers due to voids in the sheath hub that may prevent proper guidewire placement. Users may experience procedure delays and need to exchange equipment.
Product
MINI STICK MAX 4F X 10 CM STIFF .018 SS/SS ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-751
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1346-2024·2024-03-27
Guidewire Introducer Sheath from Angiodynamics Recalled for Manufacturing Defect
Angiodynamics is recalling 65 units of its MINI STICK MAX guidewire introducer sheath due to manufacturing defects that may prevent guidewires from passing through during surgical procedures.
Product
MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-775
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1335-2024·2024-03-27
Angiodynamics Guidewire Introducer Devices Recalled for Manufacturing Defects
Angiodynamics recalls MINI STICK MAX guidewire introducer devices due to manufacturing defects in the internal lumen that may prevent guidewire passage and delay surgical procedures.
Product
MINI STICK MAX 4F X 10 CM STD .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-750
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1316-2024·2024-03-27
Medtronic DLP Vessel Cannula Recalled for Incorrect Labeling
Medtronic is recalling 4,343 units of DLP Vessel Cannula (Model REF 30000) due to incorrect labeling on three manufactured lots distributed globally.
Product
Medtronic DLP Vessel Cannula, Model Number REF 30000
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-1306-2024·2024-03-27
Natus Sleep Supplies Recalled for Conductive Adhesive Gel Quality Defects
Natus Neurology is recalling Sleep Supplies Start Kits due to defective conductive adhesive gel supplied by Parker Laboratories. The gel is too thick, discolored, and caused patient irritation in at least one case.
Product
natus neurology, Sleep Supplies Start Kit with Single Use Supplies for Embla EX Series Amplifiers, REF 024252
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1315-2024·2024-03-27
Laboratory Control Material Recalled Due to Temperature Storage Excursion
Abbott Point of Care Control i-STAT Level 3 control material (Lot 121164) is being recalled due to temperature excursions in storage that could affect test accuracy. Affected units were distributed in Arizona, Pennsylvania, and Texas.
Product
Abbott Point of Care Control Control i-STAT¿ Level 3 1.7 mL
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1339-2024·2024-03-27
Angiodynamics surgical guidewire recalled for manufacturing defect
Angiodynamics is recalling 5,176 units of MINI STICK MAX guidewires due to manufacturing voids that prevent passage through the introducer during surgery. Surgeons may need to exchange the sheath to complete procedures.
Product
MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 2.75" PG Catalog Number: 45-756
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1349-2024·2024-03-27
Landauer microStar Reader dosimetry system discontinued for medical applications
Landauer is permanently discontinuing the microStar Reader medical dosimetry system. The company is removing product documentation references and discontinuing use with medical dosimeters.
Product
microStar Reader, Model Numbers: 10015-000 (marketed in EMEA as 100, 102, 110, and 201), 10016-000 (marketed in EMEA as 101), 10036-000, 10044-000, 10055-000, BC30058, and BC30059
Category
Medical Device
Distribution
Distributed nationwide

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6951–6975 of 13666