FoodClass I
Nelson & Isa Lacteos LLC recalls Requeson (soft ricotta) 1 lb
Products may be contaminated with Listeria monocytogenes.
· FDA · NY
Recalls
Safety recalls that rarely make the news, straight from the official U.S. agency records (FDA, USDA, CPSC, NHTSA). Every listing links to its official notice. We only copy what the record says.
Checked Nov 3, 8:30 PM ET · refreshed about every 2.5 hours · RSS · Get recall alerts
State filter: shows recalls whose official distribution lists that state, plus nationwide ones. CPSC and NHTSA recalls apply nationwide.
1107 recalls
Medicines & devicesClass I
Medline Industries, LP recalls 3 products
Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in Dextrose Injection, USP. B. Braun Medical Inc. was notified by their sup
· FDA · AZ, CA, FL, IL, IN, NJ, OH, SC
Medicines & devicesClass II
GE Medical Systems, LLC recalls 3 products
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. I
· FDA · Nationwide
Medicines & devicesClass II
Olympus Corporation of the Americas recalls Olympus Single Use Distal Cover
Olympus has developed and released newly designed version of the Distal Cover (MAJ-2315) to replace previous design of the Single Use Distal Covers.
· FDA · Nationwide
Medicines & devicesClass II
Integra LifeSciences Corp. (NeuroSciences) recalls OmniTract Surgical Retractor System
The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Integra LifeSciences has identified that the dry time needs to be extended to 90 minutes, 110 minutes, or 120 minutes depending on the
· FDA · Nationwide
Medicines & devicesClass II
Medela Inc recalls Brand Name: Medela Product Name: ENFit ExSet Strl 60 2
May contain incorrect connectors and will not attach or misconnect to ENFit connections and is thus incompatible. Issue could lead to slight delay in delivery of enteral nutritional fluids or oral medication.
· FDA · 18 states
FoodClass IUpdated
La Colonia Foods Llc recalls 4 products
Products may be contaminated with Listeria monocytogenes.
· FDA · MD, VA
FoodClass II
W.Y. Industries, Inc. recalls WY Duck Sauce
Product may contain metal fragments.
· FDA · NJ, NY, OH, PA
Medicines & devicesClass II
Lupin Pharmaceuticals Inc. recalls prednisoLONE Acetate Ophthalmic Suspension
Presence of Foreign Substance
· FDA · Nationwide
Medicines & devicesClass II
Spacelabs Healthcare, Inc. recalls Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 Software Version: N/A Prod
Due to off-the-shelf display port component that has audio/video failures
· FDA · Nationwide
Medicines & devicesClass II
Biomerieux Inc recalls VITEK 2 AST-N447 TEST KIT Product reference 424620
Potential for false resistant carbapenem and/or cephalosporin results when analyzing samples with kits from affected lot that have pouch foil fractures.
· FDA
Medicines & devicesClass II
BD SWITZERLAND SARL recalls MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number: SAM2461 UDI code: N/A Engineeri
Due to engineering sample labeled "Not for Human Use" being inadvertently shipped it the U.S. market.
· FDA · IL
Medicines & devicesClass II
Penumbra, Inc. recalls Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT
Due to manufacturing issues, reperfusion catheters may fractures
· FDA · Nationwide
Medicines & devicesClass II
Remel, Inc recalls GC Agar Base (150mm) 10/PK R04030
Reduced or no recovery of some strains of Neisseria gonorrhoeae.
· FDA · Nationwide
FoodClass IIIUpdated
Shandong Ling Xian Food Co.,LTD recalls 3 products
Undeclared sodium tripolyphosphate (STTP)
· FDA · CA
Medicines & devicesClass II
Maquet Cardiovascular, LLC recalls The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000
Getinge identified that Vasoview Hemopro 2 devices from Lot 3000547797 were exposed to an out-of-specification sterilization dose during a gamma sterilization run (Run ID 1183-28782A) performed by STERIS at its Whippany,
· FDA · Nationwide
FoodClass IUpdated
Clover Hill Dairy, LLC recalls 18 products
Product contaminated with Listeria monocytogenes.
· FDA · MD, NY, VA
Medicines & devicesClass III
SUN PHARMACEUTICAL INDUSTRIES INC recalls Fexofenadine Hydrochloride Tablets
Failed Impurities/Degradation Specifications
· FDA · Nationwide
Medicines & devicesClass I
Argon Medical Devices, Inc recalls 6 products
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 · Nationwide
Medicines & devicesClass II
Carl Zeiss Meditec AG recalls Zeiss Intrabeam Spherical Applicator 1
Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications.
· FDA · Nationwide
FoodClass I
Synear Foods USA, LLC Recalls Frozen Pork and Crab Soup Dumpling Products Due to Misbranding and Undeclared Allergens
High - Class I · Class I
· USDA FSIS · CA, NJ, WA
Medicines & devicesClass II
Gasco Industrial Corp. recalls 6 products
Subpotent drug
· FDA · Nationwide
Medicines & devicesClass II
Emano Metrics, Inc. recalls Emano Flow with software version v2
Problem description/Reason for recall: During the period March 22, 2026, to May 29, 2026, recorded urination audio was captured at 48,000 Hz while the model was trained and validated on 44,100 Hz audio. The models depend
· FDA · Nationwide
Medicines & devicesClass I
Hamilton Medical AG recalls Breathing circuit set
Ventilator coaxial breathing circuit may have, expiratory valve sets with membranes sticking to valve body, not detectable during pre-operative test, which will result in "exhalation obstructed " alarm, which may result
· FDA · Nationwide
FoodClass II
Wise Foods Inc recalls Wise Onion Rings
The product contains undeclared Yellow 5 and 6, Blue 1, and unapproved Red 3.
· FDA · FL, NC, NJ, NY, PA, SC, VA
FoodClass II
Specialty Bakers, LLC recalls Vanilla Dessert Shells (Giant)
Undeclared Allergen (Soy)
· FDA · PA
Medicines & devicesClass II
SEASPINE ORTHOPEDICS CORPORATION recalls SeaSpine Polyaxial Head REF Number: 41-3010
Due to manufacturing error, polyaxial head may popoff from the screw intraoperatively following insertion.
· FDA · Nationwide
Medicines & devicesClass II
Medline Industries, LP recalls 3 products
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 d
· FDA · Nationwide
Medicines & devicesClass II
Medline Industries, LP recalls 8 products
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances
· FDA · Nationwide
Medicines & devicesClass II
Medtronic MiniMed, Inc. recalls MiniMed 780G Insulin Pump
A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and displays two error messages back-to-back: Pump Error 53 follo
· FDA
Recall data comes from official U.S. government sources: openFDA (food, drugs, devices), USDA FSIS (meat, poultry, egg products), CPSC (consumer and children’s products) and NHTSA (vehicles, equipment, car seats). openFDA notes its data should not be relied on for medical decisions. Always confirm with the official notice. Check your vehicle by VIN at nhtsa.gov/recalls.