All Recalls

92,900 total recalls in our database

Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.

Feb 11, 2025 Other Medical Devices Nationwide View Details →

Aspiration system, for endoscopic examination/treatment of urinary tract and kidney interior, to have labeling update adding additional instructions, for patients with high viscosity fluid in the kidney, not to continue providing fluid inflow in the presence of unresolved slow or absent fluid outflow because this can create intrarenal pressure imbalance, and lead to excessive intrarenal pressure.

Feb 19, 2025 Other Medical Devices Nationwide View Details →

Medline procedure kits labeled as: 1) ANGIO DRAPE PACK (DRLUL)-LF, Pack Number DYNJ47718D; 2) ANGIO PACK, Pack Number DYNJ69678; 3) ANGIOGRAPHY CV RAD PACK, Pack Number DYNJ64936A; 4) ANGIOGRAPHY DRAPE PACK, Pack Number DYNJ49621C; 5) ANGIOGRAPHY PACK, Pack Number DYNJ61266A; 6) ANGIOGRAPHY PACK-LF, Pack Number DYNJ35916N; 7) ARTERIOGRAM PACK, Pack Number DYNJ34442F; 8) CARDIAC CATH FEMORAL PACK, Pack Number DYNJ53588I; 9) CARDIAC CATH PACK, Pack Number DYNJ31733C; 10) CARDIAC CATH PACK, Pack Number DYNJ41315A; 11) CARDIAC CATH PACK-LF, Pack Number DYNJ0380198L; 12) CATH LAB PACK, Pack Number 0M-CP31796Q; 13) CATH LAB PACK-LF, Pack Number DYNJ0194968AG; 14) CATH LAB TRAY, Pack Number 00-401610J; 15) CHRISTUS SR CATH LAB PACK, Pack Number DYNJ60931C; 16) CRMC CATH LAB TRAY JUDKINS-LF, Pack Number DYNJ61088F; 17) CRMC NEURO ENDO HYBRID-LF, Pack Number DYNJ61101D; 18) EP PACK MORNINGSIDE, Pack Number DYNJ69301; 19) FEMORAL TRAY 2, Pack Number DYNJ68812C; 20) INTERVENTIONAL MINOR PACK, Pack Number DYNJ24615D; 21) INTERVENTIONAL PACK, Pack Number DYNJ54253; 22) INTERVENTIONAL RADIOLOGY PK-LF, Pack Number PHS605358025B; 23) MORNINGSIDE CARDIAC CATH, Pack Number DYNJ58339A; 24) OR INTERVENTIONAL PACK, Pack Number DYNJ46934A; 25) PACK,CARDIAC CATH, Pack Number DYNJ65481; 26) PK, RADIOLOGY-SPECIALS, Pack Number DYNJ59628C; 27) PTCA TRAY-LF, Pack Number DYNJ07252V; 28) RADIOLOGY PACK, Pack Number DYNJ45393A; 29) RR-ANGIOGRAPHY DRAPE PACK-LF, Pack Number DYNJ0608549M; 30) SPEC ANGIO PACK (SASJK)642-LF, Pack Number DYNJ47586F; 31) SPECIALS LINE PACK, Pack Number DYNJ69504; 32) TV-CARDIAC CATH PACK-LF, Pack Number DYNJ41564P; 33) TV-CARDIAC CATH PACK-LF, Pack Number DYNJ41564P; 34) UTHET TYLER ELECTROPHYSIOLOGY, Pack Number DYNJ68672C

MEDLINE INDUSTRIES, LP - Northfield

🏥 Medical Devices Class I - Dangerous

Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.

Feb 11, 2025 Other Medical Devices Nationwide View Details →

George Oliver Dressers

Zhangzhou Jiesi Intelligent Technology Co. Ltd., of China

🏠 Consumer Products Class II - Moderate

The recalled dressers are unstable if they are not properly anchored to the wall, posing serious tip-over and entrapment hazards, and the two additional metal support legs also present tripping hazards. The dressers violate performance and warning label requirements of the STURDY Act.

Mar 27, 2025 Furniture Nationwide View Details →

Children's Steel Utility Bunk Beds

Delweld Industries Corp., of Stoystown, Pennsylvania

🏠 Consumer Products Class II - Moderate

The recalled children's bunk beds violate the federal regulations for bunk beds because the spacing between the guardrail and end support and the spacing around the mattress supports are greater than allowed, posing entrapment and strangulation hazards to children.

Mar 27, 2025 Furniture Nationwide View Details →
🏠 Consumer Products Class II - Moderate

The recalled jewelry-making kits contain a resin that, when liquid, can cause skin, eye and respiratory irritation or sensitization when inhaled, touched or ingested. The resin contains an acrylate (hydroxyethylmethacrylate "HEMA") in amounts prohibited in children's products by the Federal Hazardous Substances Act. Already created jewelry should be inspected to confirm it is fully cured. If there is liquid or any liquid residue present, the jewelry should not be worn and should be stored away from children. Once cured, the resin no longer presents the hazard.

Mar 27, 2025 Clothing & Accessories Nationwide View Details →
🏠 Consumer Products Class I - Dangerous

The recalled window shades have long operating cords that can cause death or serious injury to children, due to strangulation and entanglement hazards. The window shades are in violation of the federal regulations for window coverings and present a substantial product hazard. The window shades also violate federal regulations for labeling of window coverings.

Mar 27, 2025 Other Consumer Products Nationwide View Details →

NFH Iron SAP, NFH Heme Iron SAP and NFH Prenatal SAP bottles

Nutritional Fundamentals for Health (dba NFH), of Canada

🏠 Consumer Products Class II - Moderate

The recalled dietary supplements contain iron, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The packaging is not child-resistant, posing a risk of poisoning if the contents are swallowed by young children.

Mar 27, 2025 Other Consumer Products Nationwide View Details →