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 the agency’s own highest classification or reported deaths or serious injuries, 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

15176–15200 of 27471

HighFDA (Devices)·Z-0008-2020·2019-10-09
Baxter ExactaMix IV Bags Recalled for Potential Leaking
The Metrix Company is recalling Baxter ExactaMix IV bags due to a potential for leaking. The recall covers 332,640 units distributed nationwide.
Product
ExactaMix, Model: H938905, EMPTY EVA DUAL CHAMBER CONTAINER With Screw Connectors, 250 ml/ 1250 ml, Baxter - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2716-2019·2019-10-09
Medtronic Recalls SHERPA NX Active Guiding Catheters Due to Material Loss
Medtronic Vascular is recalling 10 units of SHERPA NX Active Guiding Catheters because a defect may expose underlying stainless-steel braid wires.
Product
SHERPA NX ACTIVE GUIDING CATHETER, 6F FR4.0, .070", REF SA6FR40. for cardiovascular use
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2584-2019·2019-10-09
Medtronic Vascular Recalls Sherpa NX Active Guiding Catheters
Medtronic Vascular is recalling 53 units of Sherpa NX Active Guiding Catheters due to a potential loss of primary segment material that could expose underlying stainless-steel braid wires.
Product
SHERPA NX ACTIVE GUIDING CATHETER, 6F, IMA, 90CM, 070", REF SA6IMAD . for cardiovascular use
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2613-2019·2019-10-09
Medtronic Recalls Six Sherpa NX Active Guiding Catheters
Medtronic Vascular is recalling six units of the Sherpa NX Active Guiding Catheter due to a potential loss of primary segment material that could expose underlying stainless-steel braid wires.
Product
SHERPA NX ACTIVE GUIDING CATHETER, 6F SR3.5, .070" REF SA6SR35. for cardiovascular use
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2637-2019·2019-10-09
Medtronic Recalls Sherpa NX Active Guiding Catheters for Material Loss
Medtronic Vascular is recalling specific Sherpa NX Active Guiding Catheters due to a potential loss of material that could expose underlying stainless-steel wires.
Product
SHERPA NX ACTIVE GUIDING CATHETER, 6F SCR4.0 SH, .070", REF SA6SCR40SH. for cardiovascular use
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0035-2020·2019-10-09
Quality Electrodynamics Recalls 15CH Knee Coils Due to Ferrous Material
Quality Electrodynamics LLC is recalling five Siemens 15CH Knee Coils because unintended ferrous material may be present in the pushbutton assembly.
Product
TxRx 15CH Knee Coil 3T QED part number: Q7000051 Siemens Model # 10606525
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-2644-2019·2019-10-09
Medtronic Recalls Sherpa NX Active Guiding Catheters Due to Material Loss
Medtronic Vascular is recalling 353 units of Sherpa NX Active Guiding Catheters because a defect may expose underlying stainless-steel braid wires.
Product
SHERPA NX ACTIVE GUIDING CATHETER, 6F JR3.5 SH, .070", REF SA6JR35SH. for cardiovascular use
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0006-2020·2019-10-09
Metrix Secure EVA IV Bags Recalled for Potential Leaking
The Metrix Company is recalling 54,720 Secure EVA dual chamber IV bags due to a potential for leaking. The affected units were distributed in the US and Canada.
Product
SECURE EVA - DUAL CHAMBER CONTAINER with Manifold, 4000mL, REF 66641 (Canadian distribution) - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0007-2020·2019-10-09
FDA Recalls ExactaMix IV Bags Due to Potential Leaking
The FDA is recalling 175,392 ExactaMix IV bags due to a potential for leaking. The bags are used for intravenous admixture programs.
Product
ExactaMix, Model: H938901, EMPTY EVA DUAL CHAMBER CONTAINER With Screw Connectors, 500 ml/ 2500 ml, Baxter - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2761-2019·2019-10-09
Helena Laboratories Recalls Cascade Abrazo aPTT Test Cards for Export
Helena Laboratories is recalling 21 kits of Cascade Abrazo aPTT Test Cards, Model 5722, distributed to Germany and Australia, due to potential false negative results.
Product
Cascade Abrazo aPTT Test Card, Model 5722, For Export Only. The firm name on the label is Helena Laboratories, Beaumont, TX.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0003-2020·2019-10-09
Metrix Secure EVA IV Bags Recalled for Potential Leaking
The Metrix Company is recalling 1,512 Secure EVA dual chamber IV bags due to a potential for leaking. The affected bags were distributed nationwide in the US.
Product
SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors, 4000mL, (legless) REF 66640 - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0031-2020·2019-10-09
Quality Electrodynamics Recalls Two Siemens Knee Coils Due to Ferrous Material
Quality Electrodynamics LLC is recalling two Siemens knee coils because unintended ferrous material may be present in the pushbutton assembly.
Product
TxRx 15Ch Knee Coil 3T QED part number:Q7000008 Siemens Model # 10185460
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-2728-2019·2019-10-09
Medtronic Recalls Sherpa NX Active Guiding Catheters Due to Material Loss
Medtronic Vascular is recalling 9 units of Sherpa NX Active Guiding Catheters because primary segment material may be lost, exposing underlying stainless-steel braid wires.
Product
SHERPA NX ACTIVE GUIDING CATHETER, 6F SCR5.0, .070", REF SA6SCR50. for cardiovascular use
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2667-2019·2019-10-09
Medtronic Recalls Six Sherpa NX Active Guiding Catheters
Medtronic Vascular is recalling six units of the Sherpa NX Active Guiding Catheter due to a potential loss of segment material that could expose underlying stainless-steel braid wires.
Product
SHERPA NX ACTIVE GUIDING CATHETER, 6F RBU4.5, .070", REF SA6RBU45. for cardiovascular use
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2699-2019·2019-10-09
Medtronic Recalls Sherpa NX Active Guiding Catheters Due to Material Loss
Medtronic Vascular is recalling 6 units of Sherpa NX Active Guiding Catheters because primary segment material may be lost, exposing underlying stainless-steel braid wires.
Product
SHERPA NX ACTIVE GUIDING CATHETER, 6F EL GAMAL SH, .070", REF SA6ELGAMALSH. for cardiovascular use
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0002-2020·2019-10-09
Metrix Secure EVA Dual Chamber Container Recall for Leaking
The Metrix Company is recalling 4,284 Secure EVA dual chamber containers due to a potential for leaking. The affected bags are used for intravenous admixtures.
Product
SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors, 3000mL, (legless) REF 66630 - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2636-2019·2019-10-09
Medtronic Recalls Sherpa NX Active Guiding Catheters for Material Loss
Medtronic Vascular is recalling 61 units of Sherpa NX Active Guiding Catheters due to a potential loss of primary segment material that could expose underlying stainless-steel braid wires.
Product
SHERPA NX ACTIVE GUIDING CATHETER, 6F M RESS, .070", REF SA6MRESS. for cardiovascular use
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2645-2019·2019-10-09
Medtronic Recalls Sherpa NX Active Guiding Catheters Due to Material Loss
Medtronic Vascular is recalling 248 units of Sherpa NX Active Guiding Catheters because primary segment material may be lost, exposing underlying stainless-steel braid wires.
Product
SHERPA NX ACTIVE GUIDING CATHETER, 6F RCB, .070", REF SA6RCB. for cardiovascular use
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2705-2019·2019-10-09
Medtronic Recalls Sherpa NX Active Guiding Catheters Due to Material Loss
Medtronic Vascular is recalling 27 units of the Sherpa NX Active Guiding Catheter because the primary segment material may break, exposing stainless-steel braid wires.
Product
SHERPA NX ACTIVE GUIDING CATHETER, 6F SAL1.0 SH, .070", REF SA6SAL10SH. for cardiovascular use
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0005-2020·2019-10-09
Metrix Secure EVA Dual Chamber IV Bags Recalled for Leaking
The Metrix Company is recalling 234,720 Secure EVA dual chamber IV bags due to a potential for leaking. The affected units were distributed nationwide in the US.
Product
SECURE EVA - DUAL CHAMBER CONTAINER with Manifold, 3000mL, REF 66631 (Canadian distribution) - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0034-2020·2019-10-09
Quality Electrodynamics Recalls 3 Siemens Knee Coils Due to Ferrous Material
Quality Electrodynamics LLC is recalling three Siemens 1.5T Knee Coils because unintended ferrous material may be present in the pushbutton assembly.
Product
TxRx 15CH Knee Coil 1.5T QED part number: Q7000050 Siemens Model # 10606524
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-2685-2019·2019-10-09
Medtronic Recalls Sherpa NX Active Guiding Catheters Due to Material Loss
Medtronic Vascular is recalling 57 units of Sherpa NX Active Guiding Catheters due to a potential loss of primary segment material that could expose underlying stainless-steel braid wires.
Product
SHERPA NX ACTIVE GUIDING CATHETER, 6F RCB SH, .070", REF SA6RCBSH. for cardiovascular use
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2552-2019·2019-10-02
Sentinel CH SpA Recalls Alinity c Lithium Reagent Kits
Sentinel CH SpA is recalling Alinity c Lithium Reagent Kits due to a potential carryover issue that may result in falsely elevated lithium patient results.
Product
Alinity c Lithium Reagent Kit- intended for the quantitation of lithium in serum or plasma using respectively the ARCHITECT c Systems and the Alinity c analyzer List Number: 08P5320
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2561-2019·2019-10-02
Elekta Monaco RTP System Recalled for Potential Dose Calculation Errors
Elekta Inc is recalling 49 Monaco RTP Systems because unintentional changes to electron density settings may cause incorrect dose calculations for radiation therapy plans.
Product
Monaco RTP System, 5.50/5.51, radiation treatment planning system Product Usage: The Monaco system is used to make treatment plans for patients with prescriptions for external beam radiation therapy. The system calculates dose for photon, electron, and carbon treatment plans…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2756-2019·2019-10-02
Medline Electric Surgical Clipper Recalled for Overheating Charger Base
Medline Industries is recalling 500 electric surgical clippers because a defective circuit board component may cause the charger base to overheat and malfunction.
Product
MEDLINE ELECTRIC SURGICAL CLIPPER AND BASE, REF DYND70800 Product Usage: Medline Surgical Clipper is intended for the removal of body hair from the patient as required prior to surgery or other minor procedures.
Category
Medical Device
Distribution
Distributed nationwide

How to read this listing

Filters

15176–15200 of 27471