Latest Product Recalls Today

Recent Product Recall Alerts List

Showing 1,476 - 1,500 of 4,622 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Ice Pop, D'Dioses Cookies Cream, 1 Bar (81.7 g), with UPC 710594511362 May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.	FDA H-1167-2026	Food	High	Jul 22, 2026 Recall: May 4, 2026	Details
Ice Pop, D'Dioses Limon, 4 oz (85 g), with UPC 710594511836 May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.	FDA H-1169-2026	Food	High	Jul 22, 2026 Recall: May 4, 2026	Details
Ice Pop, D'Dioses Mango, 3.7 oz (81.7 g), with UPC 827912008494 May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.	FDA H-1171-2026	Food	High	Jul 22, 2026 Recall: May 4, 2026	Details
Ice Pop, D'Dioses Fresa Leche, 4 oz (85 g), with UPC 710594511850 May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.	FDA H-1159-2026	Food	High	Jul 22, 2026 Recall: May 4, 2026	Details
Ruby, Artichoke Hearts Quartered, 5 LB 8 OZ (2500 G) DRAINED WT 3 LBS 6 OZ (1550G), Can, 6 cans per case, Store in dry conditions . Foreign material (Glass) was found in the product.	FDA H-1176-2026	Food	High	Jul 22, 2026 Recall: May 15, 2026	Details
OLA-OLA POUNDED GROUNDNUTS (INTWILO) NET WT. 32 oz., 2 lbs. (0.907 kg) Distributed by: Yusol International Foods Sacramento, CA 95828 Product of USA INGREDIENTS: Pounded Groundnuts (Intwilo) UPC: 650655764330 Undeclared peanuts	FDA H-1175-2026	Food	High	Jul 22, 2026 Recall: Jun 19, 2026	Details
Ice Pop, D'Dioses Arroz con Leche, 4 oz (85 g), with UPC 710594511843 May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.	FDA H-1160-2026	Food	High	Jul 22, 2026 Recall: May 4, 2026	Details
functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY NET WT. 12 OZ (341g) case UPC 8 57858 00453 3, package UPC 8 57858 00450 2 Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.	FDA H-1152-2026	Food	High	Jul 22, 2026 Recall: May 26, 2026	Details
Ice Pop, D'Dioses Tamarindo, 1 Bar (81.7 g), with UPC 827912008593 May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.	FDA H-1172-2026	Food	High	Jul 22, 2026 Recall: May 4, 2026	Details
Ice Pop, D'Dioses Nuez, 1 Bar (81.7 g), with UPC 827912008548 May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.	FDA H-1166-2026	Food	High	Jul 22, 2026 Recall: May 4, 2026	Details
ABIOMED Introducer Kit 23 Fr, 11 cm, Pump Set Code 1000441, containing Kit, 23Fr Introducer, 11cm, Sterile, Introducer Product Code 2000342. heart pump and accessories A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.	FDA Z-2684-2026	Medical Device	High	Jul 22, 2026 Recall: Jun 11, 2026	Details
Bone Marrow Tray, REF: CB0033TL; CB0355TLA Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.	FDA Z-2709-2026	Medical Device	High	Jul 22, 2026 Recall: Jun 1, 2026	Details
ABIOMED Impella CP Smart Assist Set, JP, Pump Set Code 0048-0024-JP; containing Introducer Product Code 0052-3025-JP. heart pump and accessories A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.	FDA Z-2690-2026	Medical Device	High	Jul 22, 2026 Recall: Jun 11, 2026	Details
ABIOMED Intro Kit, 14Fr x 13 and 25 cm, PKGD, JP, Pump Set Code 0052-0023-JP; containing Introducer Product Code 0052-3025-JP. heart pump and accessories A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.	FDA Z-2693-2026	Medical Device	High	Jul 22, 2026 Recall: Jun 11, 2026	Details
ABIOMED Impella 5.5 Smart Assist Set, JP, Pump Set Codes 1000211, 1000212; containing Introducer Product Code 0052-3006-JP. heart pump and accessories A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.	FDA Z-2687-2026	Medical Device	High	Jul 22, 2026 Recall: Jun 11, 2026	Details
Abiomed REF: 0052-3006, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Infusion Sideport, 23F. heart pump and accessories. Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub region.	FDA Z-2680-2026	Medical Device	High	Jul 22, 2026 Recall: Jun 10, 2026	Details
ABIOMED Impella CP Set, Pump Set Code 0048-0044; containing Introducer Product Code 0052-3046. heart pump and accessories A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.	FDA Z-2691-2026	Medical Device	High	Jul 22, 2026 Recall: Jun 11, 2026	Details
Brand Name: Rio" II Product Name: Rio" II Nasal Pillows Interface Model/Catalog Number: RII1001 (Small), RII1002 (Medium), RII1003 (Large) Software Version: N/A Product Description: Nasal pillows interface intended for use with positive airway pressure therapy devices. The device delivers airflow from a PAP device to the patient's nose and is secured using adjustable headgear. Component: No Packaging and labeling discrepancy involving product size identification and associated Unique Device Identifier (UDI/GTIN).	FDA Z-2740-2026	Medical Device	High	Jul 22, 2026 Recall: Jun 15, 2023	Details
ABIOMED Impella RP Flex with SmartAssist Set, Pump Set Code 1000323, containing Kit, 23Fr Introducer, 11cm, Sterile, 23 Fr, 11 cm, Product Code 2000342. heart pump and accessories A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.	FDA Z-2681-2026	Medical Device	High	Jul 22, 2026 Recall: Jun 11, 2026	Details
Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.	FDA Z-2738-2026	Medical Device	High	Jul 22, 2026 Recall: May 25, 2026	Details
da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13, 430013-15 Robotic-assisted surgical system arm drapes may detach from the instrument arm due to an issue involving the drape rings located at the top of the product, which may expose a section of instrument arm, which may result in procedure delay or conversion to an alternate minimally invasive approach. Retrospectively reported recall.	FDA Z-2722-2026	Medical Device	High	Jul 22, 2026 Recall: May 12, 2025	Details
Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK-LF DYNJ61651J Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach. Health consequences from use of product include clinically insignificant extension of surgery to find another readily available device.	FDA Z-2737-2026	Medical Device	High	Jul 22, 2026 Recall: Jun 10, 2026	Details
Olympus Toomey Evacuator 50cc with Adaptor. Model Number: 188A. Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to sterilize the devices.	FDA Z-2719-2026	Medical Device	High	Jul 22, 2026 Recall: May 5, 2026	Details
Orthofix MINIRAIL, SHORT, LENGTHENER REF: M103, Unilateral orthopedic/trauma external fixation device Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111	FDA Z-2730-2026	Medical Device	High	Jul 22, 2026 Recall: Jun 10, 2026	Details
Optima XR240amx, Mobile Digital Radiographic System GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety pawl may not have been performed to confirm proper assembly. If a failure of the internal counterpoise cable occurs, the Column Safety mechanism will not work, causing the arm with X-ray tube and collimator to drop downward on the column track. This could result in patient injury during an exam.	FDA Z-2728-2026	Medical Device	High	Jul 22, 2026 Recall: Jun 5, 2026	Details

Showing 1,476 - 1,500 of 4,622 product recalls

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