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.

Agency

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

1026–1050 of 13390

HighFDA (Devices)·Z-1174-2026·2026-02-04
[pending] Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R; Siemens Material Number (SMN): 1157400
Pending LLM rewrite. Source: FDA_DEVICE Z-1174-2026.
Product
Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R; Siemens Material Number (SMN): 11574002; With Software Version VB10D-SP02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1115-2026·2026-02-04
[pending] Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number:
Pending LLM rewrite. Source: FDA_DEVICE Z-1115-2026.
Product
Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700RE Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1189-2026·2026-02-04
[pending] Medline medical procedure convenience kits labeled as: 1) BREAST-HERNIA-PORT CDS-LF, Kit SKU CDS9
Pending LLM rewrite. Source: FDA_DEVICE Z-1189-2026.
Product
Medline medical procedure convenience kits labeled as: 1) BREAST-HERNIA-PORT CDS-LF, Kit SKU CDS984853L; 2) BREAST BIOPSY PACK, Kit SKU DYNJ45641B; 3) DERMATOLOGY PACK, Kit SKU DYNJT3658A.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1191-2026·2026-02-04
[pending] Medline medical procedure convenience kits labeled as: 1) SMJ LAP CHOLE PACK-LF, Kit SKU DYNJ1997
Pending LLM rewrite. Source: FDA_DEVICE Z-1191-2026.
Product
Medline medical procedure convenience kits labeled as: 1) SMJ LAP CHOLE PACK-LF, Kit SKU DYNJ19974P; 2) DEPAUL ABDOMINAL ENDOSCOPY-LF, Kit SKU DYNJ20027K; 3) LAPAROSCOPY PACK-LF, Kit SKU DYNJ20468J; 4) SMJ LAPAROSCOPY PACK, Kit SKU DYNJ25763N; 5) SMJ LAPAROSCOPY PACK,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1204-2026·2026-02-04
[pending] Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148, (2) 782116. MR systems with SW version
Pending LLM rewrite. Source: FDA_DEVICE Z-1204-2026.
Product
Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148, (2) 782116. MR systems with SW version R11.1 and R12.1.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1167-2026·2026-02-04
[pending] Fixone Biocomposite Anchor
Pending LLM rewrite. Source: FDA_DEVICE Z-1167-2026.
Product
Fixone Biocomposite Anchor
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1220-2026·2026-02-04
[pending] BEAR Implant. Model Number: 1000.
Pending LLM rewrite. Source: FDA_DEVICE Z-1220-2026.
Product
BEAR Implant. Model Number: 1000.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1166-2026·2026-02-04
[pending] Fixone Hybrid Anchor
Pending LLM rewrite. Source: FDA_DEVICE Z-1166-2026.
Product
Fixone Hybrid Anchor
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1195-2026·2026-02-04
[pending] Medline medical procedure convenience kits labeled as: 1) INPATIENT CTRL LN DRG CHG, Kit SKU DT22
Pending LLM rewrite. Source: FDA_DEVICE Z-1195-2026.
Product
Medline medical procedure convenience kits labeled as: 1) INPATIENT CTRL LN DRG CHG, Kit SKU DT22880; 2) ADULT CVC DRSG CHG W/ADHESIVE, Kit SKU DYNDC3283A.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1194-2026·2026-02-04
[pending] Medline medical procedure convenience kits labeled as: HEAD SHAVE-LATEX SAFE KIT, Kit SKU P903933B
Pending LLM rewrite. Source: FDA_DEVICE Z-1194-2026.
Product
Medline medical procedure convenience kits labeled as: HEAD SHAVE-LATEX SAFE KIT, Kit SKU P903933B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1193-2026·2026-02-04
[pending] Medline medical procedure convenience kits labeled as: 1) DRAWER 1 AIRWAY, Kit SKU ACC010270A;
Pending LLM rewrite. Source: FDA_DEVICE Z-1193-2026.
Product
Medline medical procedure convenience kits labeled as: 1) DRAWER 1 AIRWAY, Kit SKU ACC010270A; 2) DRAWER 2, Kit SKU ACC010690; 3) DRAWER 3 SYR/DRS/MON/NG 1 OF 3, Kit SKU ACC011073; 4) HYPOSPADIUS PACK, Kit SKU DYNJ00282Q; 5) SJ NEURO PACK RFID-LF, Kit SKU DYNJ0101360K;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1202-2026·2026-02-04
[pending] Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 3200TS Tourniquet Systems Model/Catalo
Pending LLM rewrite. Source: FDA_DEVICE Z-1202-2026.
Product
Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 3200TS Tourniquet Systems Model/Catalog Number: 60320010100 Software Version: Software version v2.06 or prior are within scope of the recall for A.T.S.¿ 3200TS Product Description: A.T.S 3200TS Tourniquet Systems Co
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1207-2026·2026-02-04
[pending] Ingenia 3.0T. Product Code (REF): (1) 781342, (2) 781377. MR systems with SW version R11.1 and R
Pending LLM rewrite. Source: FDA_DEVICE Z-1207-2026.
Product
Ingenia 3.0T. Product Code (REF): (1) 781342, (2) 781377. MR systems with SW version R11.1 and R12.1.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1213-2026·2026-02-04
[pending] MR 7700. Product Code (REF): (1) 782120, (2) 782153. MR systems with SW version R11.1 and R12.1.
Pending LLM rewrite. Source: FDA_DEVICE Z-1213-2026.
Product
MR 7700. Product Code (REF): (1) 782120, (2) 782153. MR systems with SW version R11.1 and R12.1.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1208-2026·2026-02-04
[pending] Ingenia 3.0T CX. Product Code (REF): 781271. MR systems with SW version R11.1 and R12.1.
Pending LLM rewrite. Source: FDA_DEVICE Z-1208-2026.
Product
Ingenia 3.0T CX. Product Code (REF): 781271. MR systems with SW version R11.1 and R12.1.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1203-2026·2026-02-04
[pending] Chest Drainage Units and Accessories: Product Code Description 1. 8888571562 Cardinal Health S
Pending LLM rewrite. Source: FDA_DEVICE Z-1203-2026.
Product
Chest Drainage Units and Accessories: Product Code Description 1. 8888571562 Cardinal Health Sentinel Seal CDU 2. 8888571513 Cardinal Health Sentinel Seal CDU, Dual Drain 3. 8888571489 Cardinal Health Sentinel Seal CDU, with Easy Change Connector 4. 8888571370 Cardinal
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1170-2026·2026-02-04
[pending] Genesis Knotless Anchor
Pending LLM rewrite. Source: FDA_DEVICE Z-1170-2026.
Product
Genesis Knotless Anchor
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1182-2026·2026-02-04
[pending] Feminine hygiene products, labeled as: KOTEX FREEDOM MAXI NO WINGS 48CT, ALWAYS THIN LINERS UNSCE
Pending LLM rewrite. Source: FDA_DEVICE Z-1182-2026.
Product
Feminine hygiene products, labeled as: KOTEX FREEDOM MAXI NO WINGS 48CT, ALWAYS THIN LINERS UNSCENTED 12 CT, ALWAYS THIN LINERS SCENTED 12CT, ALWAYS ULT.THIN WINGS REG.12/22CT, ALWAYS ULT.THIN OVER NIGHT WINGS 12/16CT, JULIE MAXI NIGHT W.WINGS 36/10CT, STAY FREE REG. 12/10CT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1212-2026·2026-02-04
[pending] Ingenia Elition X. Product Code (REF): (1) 781358, (2) 782107, (3) 782136. MR systems with SW ve
Pending LLM rewrite. Source: FDA_DEVICE Z-1212-2026.
Product
Ingenia Elition X. Product Code (REF): (1) 781358, (2) 782107, (3) 782136. MR systems with SW version R11.1 and R12.1.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1165-2026·2026-02-04
[pending] PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010
Pending LLM rewrite. Source: FDA_DEVICE Z-1165-2026.
Product
PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1183-2026·2026-02-04
[pending] Toothbrushes, labeled as: ORAL B TOOTH BRUSH SHINY CLEAN SOFT 12CT; COLGATE TOOTH BRUSH MED. 12CT;
Pending LLM rewrite. Source: FDA_DEVICE Z-1183-2026.
Product
Toothbrushes, labeled as: ORAL B TOOTH BRUSH SHINY CLEAN SOFT 12CT; COLGATE TOOTH BRUSH MED. 12CT; ADULT TOOTHPASTE W BRUSH (WHITENING) 6.4oz/24ct; ADULT TOOTHPASTE W BRUSH (ANTICAV) 6.4oz/24ct.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1205-2026·2026-02-04
[pending] Evolution Upgrade 3.0T. Product Code (REF): 782143. MR systems with SW version R11.1 and R12.1.
Pending LLM rewrite. Source: FDA_DEVICE Z-1205-2026.
Product
Evolution Upgrade 3.0T. Product Code (REF): 782143. MR systems with SW version R11.1 and R12.1.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1199-2026·2026-02-04
[pending] Medline medical procedure convenience kits labeled as: 1) C-SECTION PACK, Kit SKU DYNJ35494C; 2
Pending LLM rewrite. Source: FDA_DEVICE Z-1199-2026.
Product
Medline medical procedure convenience kits labeled as: 1) C-SECTION PACK, Kit SKU DYNJ35494C; 2) SMJ C-SECTION PACK-LF, Kit SKU DYNJ38582O; 3) RR-L&D C-SECTION PACK-LF, Kit SKU DYNJ82084F.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1177-2026·2026-02-04
[pending] Alphenix INFX-8000F, interventional fluoroscopic x-ray system
Pending LLM rewrite. Source: FDA_DEVICE Z-1177-2026.
Product
Alphenix INFX-8000F, interventional fluoroscopic x-ray system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1201-2026·2026-02-04
[pending] Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tourniquet Systems Model/Catalo
Pending LLM rewrite. Source: FDA_DEVICE Z-1201-2026.
Product
Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tourniquet Systems Model/Catalog Number: 60500010100 Software Version: Software version v2.04 or prior are within scope of the recall for A.T.S.¿ 5000TS Product Description: A.T.S 5000TS Tourniquet Systems Co
Category
Medical Device
Distribution
0 states

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1026–1050 of 13390