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

15976–16000 of 27500

HighFDA (Devices)·Z-1384-2019·2019-05-29
Beckman Coulter UniCel DxH 900 Hematology Analyzer Recall for Platelet Errors
Beckman Coulter is recalling 341 UniCel DxH 900 hematology analyzers because they may produce erroneously elevated platelet results without warning, potentially masking low platelet counts.
Product
UniCel DxH 900 Coulter Cellular Analysis System, REF number C11478 Product Usage: Note: The DxH 900 hematology analyzer is CLIA categorized under document CR180294 and is currently marketed as a member of the instrument family of the DxH 800 cleared under K140911, per FDA s…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1423-2019·2019-05-29
Zimmer GmbH Recalls 2.5x135mm AO Drills Due to Material Concerns
Zimmer GmbH is recalling 2.5x135mm AO Drills because they may be made from a different material than specified. The products were distributed to 41 US states.
Product
Drill, 2.5x135mm, AO, Item Number 502015142
Category
Medical Device
Distribution
42 states
HighFDA (Devices)·Z-1413-2019·2019-05-29
Zimmer GmbH Recalls Drill System Due to Potential Material Deviation
Zimmer GmbH is recalling Drill Sys 2.7 units because they may have been manufactured from a material different from specifications.
Product
Drill Sys 2.7, 2x105mm, stryker, Item Number 502015106
Category
Medical Device
Distribution
42 states
HighFDA (Devices)·Z-1449-2019·2019-05-29
Zimmer V-TEK IVP Step Drill Recalled for Material Specification Deviation
Zimmer GmbH is recalling V-TEK IVP step drills because they may be made from a different material than specified.
Product
V-TEK", IVP step drill 2.5-3.9x124mm, 16mm stop, AO, Item Number 502015638
Category
Medical Device
Distribution
42 states
HighFDA (Devices)·Z-1427-2019·2019-05-29
Zimmer GmbH Recalls 2.7mm Orthopedic Drills Due to Material Concerns
Zimmer GmbH is recalling specific 2.7mm orthopedic drills because an investigation found they may be made from a different material than specified.
Product
Drill for 2.7mm screw, 23mm stop, 2x103mm, AO, Item Number 502015207
Category
Medical Device
Distribution
42 states
HighFDA (Devices)·Z-1420-2019·2019-05-29
Zimmer GmbH Recalls 19mm Orthopedic Drills Due to Material Concerns
Zimmer GmbH is recalling specific 19mm orthopedic drills because they may be made from the wrong material. The devices were distributed to 38 US states.
Product
Drill, 19mm stop, 1.9x87mm, AO, Item Number 502015131
Category
Medical Device
Distribution
42 states
HighFDA (Devices)·Z-1459-2019·2019-05-29
Zimmer GmbH Recalls CBS 4.0 Countersink Due to Material Concerns
Zimmer GmbH is recalling CBS 4.0 countersinks because they may have been manufactured from a different material than specified.
Product
CBS 4.0 countersink, cannulated, 30mm stop, AO, Item Number 503004353
Category
Medical Device
Distribution
42 states
HighFDA (Devices)·Z-1473-2019·2019-05-29
Zimmer GmbH Recalls 2.7mm AO Drills Due to Material Concerns
Zimmer GmbH is recalling 2.7x125mm AO drills because they may be made from the wrong material. The devices were distributed to 40 US states.
Product
Drill, 2.7x125mm, AO , Item Number ST502015217
Category
Medical Device
Distribution
42 states
HighFDA (Devices)·Z-1424-2019·2019-05-29
Zimmer GmbH Recalls Stryker 26mm Drill Due to Material Concerns
Zimmer GmbH is recalling Stryker 26mm drills because they may be made from the wrong material. The products were distributed to 39 US states.
Product
Drill, 26mm stop, 1.4x94mm, stryker, Item Number 502015145
Category
Medical Device
Distribution
42 states
HighFDA (Devices)·Z-1439-2019·2019-05-29
Zimmer GmbH Recalls Cannulated Drills Due to Material Specification Concerns
Zimmer GmbH is recalling specific cannulated drills because an investigation found they may have been manufactured from a different material than defined in specifications.
Product
Drill, cannulated, 2.5x95mm, AO, Item Number 502015621
Category
Medical Device
Distribution
42 states
HighFDA (Devices)·Z-1368-2019·2019-05-29
Roche Cobas infinity Software Recall for Missing Quality Control Alarms
Roche Diagnostics is recalling 15 units of Cobas infinity software versions 2.0 through 2.5 because quality control alarms may fail to display after a bottle change.
Product
Cobas¿ infinity central lab IT solution Material Number: 07154003001 Calculator/Data Processing Module, For Clinical Use
Category
Medical Device
Distribution
11 states
HighFDA (Devices)·Z-1435-2019·2019-05-29
Zimmer GmbH Recalls Cannulated Drills Due to Material Specification Concerns
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the defined specifications.
Product
Drill, cannulated, 4x120mm, AO, Item Number 502015402
Category
Medical Device
Distribution
42 states
HighFDA (Devices)·Z-1453-2019·2019-05-29
Zimmer GmbH Recalls CBS 7.5 Tap Due to Material Concerns
Zimmer GmbH is recalling CBS 7.5 taps because they may be made from the wrong material. The products were distributed to 41 US states.
Product
CBS 7.5 tap, cannulated, AO, Item Number 503002041
Category
Medical Device
Distribution
42 states
HighFDA (Devices)·Z-1476-2019·2019-05-29
Zimmer GmbH Recalls Cannulated Drills Due to Potential Material Deviation
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a different material than specified. The products were distributed to 41 US states.
Product
Drill, cannulated, 2x95mm, round shaft, Item Number ST502015619
Category
Medical Device
Distribution
42 states
CriticalFDA (Devices)·Z-1275-2019·2019-05-22
Ethicon Intraluminal Staplers Recalled for Insufficient Firing Stroke
Ethicon Endo-Surgery is recalling 434,614 Straight Intraluminal Staplers (Model SDH21A) because they may have an insufficient firing stroke to break the washer and completely form staples.
Product
Straight Intraluminal Staplers, 21 mm diameter, Model SDH21A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1273-2019·2019-05-22
Ethicon Endo-Surgery Recalls Endoscopic Curved Intraluminal Staplers
Ethicon Endo-Surgery is recalling 434,614 endoscopic curved intraluminal staplers because they may have an insufficient firing stroke to break the washer and completely form staples.
Product
Endoscopic Curved Intraluminal Stapler, 29 mm diameter, Model ECS29A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1277-2019·2019-05-22
Ethicon Endo-Surgery Recalls Straight Intraluminal Staplers Due to Firing Defect
Ethicon Endo-Surgery Inc is recalling 434,614 Straight Intraluminal Staplers (Model SDH29A) because they may have an insufficient firing stroke to break the washer and completely form staples.
Product
Straight Intraluminal Staplers, 29 mm diameter, Model SDH29A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1278-2019·2019-05-22
Ethicon Endo-Surgery Recalls Straight Intraluminal Staplers Due to Firing Defect
Ethicon Endo-Surgery is recalling 434,614 Straight Intraluminal Staplers (Model SDH33A) because they may have an insufficient firing stroke to break the washer and completely form staples.
Product
Straight Intraluminal Staplers, 33 mm diameter, Model SDH33A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1351-2019·2019-05-22
Molift 2-Point Sling Bar Recalled Due to Hook Breakage Risk
Moller Vital is recalling 427 Molift 2-Point sling bars because broken hooks may cause the sling to slip, potentially leading to patient falls.
Product
Molift 2-Point sling bar, an accessory for Molift Mover 205. Item nos. 1430016 1430017 1430021
Category
Medical Device
Distribution
10 states
SevereFDA (Devices)·Z-1270-2019·2019-05-22
Ethicon Curved Intraluminal Staplers Recalled for Insufficient Firing Stroke
Ethicon Endo-Surgery is recalling 434,614 Curved Intraluminal Staplers (Model CDH33A) because they may have an insufficient firing stroke to break the washer and form staples.
Product
Curved Intraluminal Staplers, 33 mm diameter, Model CDH33A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1271-2019·2019-05-22
Ethicon Endo-Surgery Recalls Endoscopic Curved Intraluminal Staplers
Ethicon Endo-Surgery is recalling 434,614 Endoscopic Curved Intraluminal Staplers because they may have an insufficient firing stroke to break the washer and completely form staples.
Product
Endoscopic Curved Intraluminal Stapler, 21 mm diameter, Model ECS21A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1268-2019·2019-05-22
Ethicon Curved Intraluminal Staplers Recalled for Insufficient Firing Stroke
Ethicon Endo-Surgery is recalling Curved Intraluminal Staplers, Model CDH25A, because they may have an insufficient firing stroke to break the washer and completely form staples.
Product
Curved Intraluminal Staplers, 25 mm diameter, Model CDH25A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1267-2019·2019-05-22
Ethicon Curved Intraluminal Staplers Recalled for Insufficient Firing Stroke
Ethicon Endo-Surgery Inc is recalling Curved Intraluminal Staplers, Model CDH21A, because they may have an insufficient firing stroke to break the washer and completely form staples.
Product
Curved Intraluminal Staplers, 21 mm diameter, Model CDH21A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1276-2019·2019-05-22
Ethicon Endo-Surgery Recalls Straight Intraluminal Staplers Due to Firing Defect
Ethicon Endo-Surgery Inc is recalling 434,614 Straight Intraluminal Staplers (Model SDH25A) because they may have an insufficient firing stroke to break the washer and completely form staples.
Product
Straight Intraluminal Staplers, 25 mm diameter, Model SDH25A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1352-2019·2019-05-22
Molift 2-Point Sling Bar Recalled Due to Hook Breakage Risk
Moller Vital is recalling Molift 2-Point sling bars because broken hooks may cause the sling to slip and patients to fall.
Product
Molift 2-Point sling bar, an accessory for Molift Mover 180/Air. Item nos. 1830001 1830002 1830002C 1830003
Category
Medical Device
Distribution
10 states

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