Safety Recalls
RSS ↗17,559 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 2,851–2,900 of 17,559
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Asymmetrical Tano Forceps, Model/Catalog Number: DVF4014-25-SField Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Class II
Medical Device Recall · March 25, 2026
Olympus Corporation of the Americas
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2138.Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Class II
Medical Device Recall · March 25, 2026
BioCera Fibers, Bioresorbable Bone Void Filler, REF: ORB-0320C-KC, ORB-0310C-KC, ORB-0304C-KC, ORB-0302C-KC, ORB-0305D-KCResorbable bone void filler falls outside standard specifications.
- Class III
Medical Device Recall · March 25, 2026
Heraeus Medical GmbH (Dental Division)
Heraeus, PALAMIX duo. Material Number: 66057897.Based on long-term stability testing, it was determined that in units older than 1.5 years (17 months) the mixing rod may, in rare cases, come loose from its lock during the mixing process. Notification is to reduce the shelf life from 3 years to 1.5 years (17 months).
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff End Grasping Forceps, Model/Catalog Number: DVF4022-25-SField Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Unclassified
Vehicle Recall · March 25, 2026
2025 ASTON MARTIN DBXUnderinflated tires increase the risk of a crash.
- Class II
Medical Device Recall · March 25, 2026
Olympus Corporation of the Americas
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2116.Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Unclassified
Vehicle Recall · March 25, 2026
Volkswagen Group of America, Inc.
2025 VOLKSWAGEN JETTA, 2025 VOLKSWAGEN TAOSAn instrument panel that does not display critical safety information, such as the speedometer or warning lights, can increase the risk of a crash.
- Unclassified
Vehicle Recall · March 25, 2026
2025 VOLVO VNL (4), 2026 VOLVO VNL (4)An instrument panel display that fails to show critical safety information, such as the speedometer or warning lights, increases the risk of a crash.
- Unclassified
Vehicle Recall · March 25, 2026
2025 VOLVO VNL (4), 2026 VOLVO VNL (4)A delayed brake release can increase the risk of crash.
- Class II
Medical Device Recall · March 25, 2026
Olympus Corporation of the Americas
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2117.Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Class II
Food Recall · March 25, 2026
Bombay Kitchen brand Tikka Sev; Net Wt 9oz (255g); INGREDIENTS: Chickpea Flour, Water, Non-GMO Expeller Pressed Canola Oil, Spices, Salt, FD&C Tomato Color and Citric Acid; CAUTION: May Contain TracesProduct(s) contain undeclared colors, FD&C Yellow #6 and FD&C Red #40
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps, Model/Catalog Number: DVF4016-25-SField Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Class II
Drug Recall · March 25, 2026
Preferred Pharmaceuticals, Inc.
Artificial Tears Lubricant Eye Drops (glycerin 0.2%, hypromellose 0.2%, polyethylene glycol 400 1%), 0.5 oz bottles, Mfg: Geri-Care; Brooklyn, New York NDC 68788-7266-0Lack of Assurance of Sterility
- Class II
Medical Device Recall · March 25, 2026
Olympus Corporation of the Americas
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2110. May be included with the Olympus OER-ELITE.Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Class III
Medical Device Recall · March 25, 2026
Heraeus Medical GmbH (Dental Division)
Heraeus, PALAMIX uno. Material Number: 66057893.Based on long-term stability testing, it was determined that in units older than 1.5 years (17 months) the mixing rod may, in rare cases, come loose from its lock during the mixing process. Notification is to reduce the shelf life from 3 years to 1.5 years (17 months).
- Class II
Medical Device Recall · March 25, 2026
Olympus Corporation of the Americas
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2111Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Class II
Drug Recall · March 25, 2026
SUN PHARMACEUTICAL INDUSTRIES INC
Fluocinonide, USP, 0.05% Cream, 60g tube, Rx only, Mfd by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1, Dist. by: Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532, NDC 51672-138Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing.
- Class II
Medical Device Recall · March 25, 2026
Olympus Corporation of the Americas
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2118.Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Class I
Medical Device Recall · March 25, 2026
Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028, LABEL, STERILE, IVSTATION SYRINGE (40MMX40MM). 2. Part Number 258900029, LABEL, STERILE, IVSTATION SYRINGEPotential for mislabeled syringe produced by the i.v.STATION device.
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 25ga DEX Nano Tapered AWH Forceps, Model/Catalog Number: DVF4005-25Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Class II
Drug Recall · March 25, 2026
SUN PHARMACEUTICAL INDUSTRIES INC
Fluocinonide, USP, 0.05% Cream, 15g tube, Rx only, Mfd by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1, Dist. by: Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532, NDC 51672-138Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing.
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019-25-SField Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Class II
Drug Recall · March 25, 2026
SUN PHARMACEUTICAL INDUSTRIES INC
Fluocinonide, USP, 0.05% Cream, 30g tube, Rx only, Mfd by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1, Dist. by: Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532, NDC 51672-138Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing.
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-27Ophthalmic Tissue Forceps (DEX") are sterile, hand-held ophthalmic surgical instruments designed for grasping, manipulating, compressing, pulling, or joining eye and/or surrounding tissues during surgical procedures. These devices fall under the GMDN code 62478 entitled Ophthalmic soft-tissue surgical forceps, probe-like, single use . Double pouched in tyvek pouches, sold in boxes of 5 with an inner and outer box.
- Class II
Medical Device Recall · March 25, 2026
ZENBONE, REF: ORB-0320C-Z, ORB-0310C-Z, ORB-0304C-ZResorbable bone void filler falls outside standard specifications.
- Class II
Medical Device Recall · March 25, 2026
Oxoid Agglutinating Sera, Salmonella 9-0 R30957301Affected lots are not performing to IFU criteria showing cross reactions with 2-0 within 60 seconds. Cross-reactivity may result in the misidentification of a Salmonella 9-O serotype as a 2-O serotype.
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-25-SField Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Class I
Medical Device Recall · March 25, 2026
VOCSN V+Pro package, REF: PRT-01198-000; VOCSN V+Pro unit, REF: PRT-01185-000Respiratory system intended to provide continuous/intermittent ventilator support, may not have been evaluated under all intended high-pressure conditions during production testing, so an oxygen leak condition could occur that may lead to reduced below intended levels of fraction of inspired oxygen delivery prior to and during ventilation and this oxygen-enriched environment may increase fire risk
- Class II
Food Recall · March 25, 2026
Bombay Kitchen brand Punjabi Mix; Net Wt 9oz (255g); INGREDIENTS: Chickpea Flour, Water, Non-GMO Expeller Pressed Canola Oil, Chana Dal (Split Bengal Gram), Brown Lentils (Masoor), Chickpeas, Rice FlaProduct(s) contain undeclared colors, FD&C Yellow #6 and FD&C Red #40
- Class II
Medical Device Recall · March 25, 2026
Olympus Corporation of the Americas
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2112Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 25ga DEX Super Grip Forceps, Model/Catalog Number: DVF4034-25Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Class II
Medical Device Recall · March 25, 2026
Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6.25cm x 1cm. Catalog Number: 1050030.Potential for product to contain foreign matter, confirmed to be inspect fragments.
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-23Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Class II
Medical Device Recall · March 25, 2026
Olympus Corporation of the Americas
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2115.XXX
- Class II
Food Recall · March 25, 2026
Crab Cakes various sizes sold to food serviceMay be temperature abused, which may result in growth of Clostridium botulinum
- Class II
Medical Device Recall · March 25, 2026
Olympus Corporation of the Americas
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2113.Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Class I
Medical Device Recall · March 24, 2026
Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038301; Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.Medline has identified the presence of particulate within the fluid path of the Manifolds.
- Class II
Drug Recall · March 24, 2026
GE Healthcare Omnipaque (iohexol) Injection, 350 mg/mL (64.7%), Rx Only, Distributed by: GE Healthcare Inc., Marlborough, MA 01752 USA, NDC 0407-1414-91.Presence of particulate matter
- Class I
Medical Device Recall · March 24, 2026
1. 3 VALVE MAN KIT, Medline Kit SKU Number: 65101544; 2. 3V MANIFOLD KIT, Medline Kit SKU Number: 65110351; 3. HEART CATH PACK-LF, Medline Kit SKU Number: DYNJ0373285M; 4. ANGIO DRAPE CARDIACMedline has identified the presence of particulate within the fluid path of the Manifolds.
- Class III
Food Recall · March 24, 2026
Garland Fresh Peeled Garlic 6 oz. bagThe potential contamination with Clostridium botulinum, due to risk of temperature abuse during chilled storage at the firm
- Class I
Medical Device Recall · March 24, 2026
Namic Preceptor Manifold, custom, Medline Product Number/SKU 64039307; Extravascular blood pressure transducerMedline has identified the presence of particulate within the fluid path of the Manifolds.
- Unclassified
Vehicle Recall · March 24, 2026
Toyota Motor Engineering & Manufacturing
2024 TOYOTA TUNDRA, 2024 TOYOTA RAV4 HYBRID, 2024 TOYOTA TUNDRA HYBRID, 2024 TOYOTA TACOMA, 2024 TOYOTA LAND CRUISER HYBRID, 2025 TOYOTA GRAND HIGHLANDER, 2025 TOYOTA RAV4 HYBRID, 2025 TOYOTA SEQUOIAA vehicle with an incorrect maximum capacity weight value may be overloaded, which can increase the risk of a crash.
- Class I
Food Recall · March 24, 2026
Fresh Cantaloupe (Whole, Fresh), brand name Ayco, wrapped in food safe plastic bags packed in corrugated cardboard cartons; 6-12 melons per box; individual carton count per label. Keep refrigerated; sPotential Salmonella Contamination
- Class I
Medical Device Recall · March 24, 2026
Namic Preceptor Manifold, custom, Medline Product Number/SKU 64037107; Extravascular blood pressure transducerMedline has identified the presence of particulate within the fluid path of the Manifolds.
- Class II
Medical Device Recall · March 24, 2026
Hintermann Series Talar Implant, Left, Size 2 REF 302112Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.
- Class III
Food Recall · March 24, 2026
SunRidge Farms Organic SUNSET SOUP MIX CERTIFIED ORGANIC BY QAI NET WT. 25 LBS Item: 013000 UPC: 086700130001Potential contamination with pesticides, haloxyfop and thiamethoxam
- Class I
Medical Device Recall · March 24, 2026
1. DBD-MTS,3V,MAN,KIT, Medline Kit Number/SKU 60010195; 2. MTS-LEFT HEART,KIT, Medline Kit Number/SKU 60033123; 3. MTS,3 VALVE,KIT, Medline Kit Number/SKU 60050183; 4. MTS,LEFT HEART,KIT, MedlinMedline has identified the presence of particulate within the fluid path of the Manifolds.
- Class I
Medical Device Recall · March 24, 2026
Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038200; Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.Medline has identified the presence of particulate within the fluid path of the Manifolds.