Recalls in Connecticut (page 19)
3932 recalls.
- MEDLINE Medical Procedure Kits labeled as: CATH 22F ROBINSON STRL 5'S PK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: ADULT TRACHEOSTOMY TUBE INSERT recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: ORAL RESTORATION recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: BILAT MICRO VASECTOMY REVERSAL recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) BNT CV PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as CH OPEN HEART recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) BASIC HEART PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: LAPAROSCOPY COMBINED - NO NDL recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Intermittent Latex Catheter Coude Pre-Connected to Collection Bag recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Intermittent Latex Catheter Coude Pre-Connected to Collection Bag recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Urethral Catheterization Tray and Bag recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Pre-connected Urethral Catheterization Tray and Bag recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Urethral Catheterization Tray recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Urethral Catheter recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - Giraffe OmniBed Field Replaceable Unit recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 24, 2026 · GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for... - Giraffe OmniBed Carestations and Giraffe OmniBed Carestation CS1 recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 24, 2026 · GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for... - Giraffe OmniBed recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 24, 2026 · GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for... - ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 12mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400. recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported June 24, 2026 · Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot... - TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300. recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported June 24, 2026 · Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot... - directCHECK ACT-LR whole blood quality control recall (Accriva Diagnostics, Inc.)
Medical deviceClass IIReported June 24, 2026 · Assayed Whole blood control contains labeling with incorrect performance range. - Medtronic O-arm O2 Imaging System. Model Number: BI70002000. recall (Medtronic Navigation, Inc.-Boxborough)
Medical deviceClass IIReported June 24, 2026 · Potential for image artifacts caused by an anomaly in the O-arm O2 Imaging System s detector panel firmware. - ALYON Surgical Lighting System recall (Steris Corporation)
Medical deviceClass IIReported June 24, 2026 · The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach. - HarmonyAIR A-Series Surgical Lighting System recall (Steris Corporation)
Medical deviceClass IIReported June 24, 2026 · The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach. - HarmonyAIR A-Series Surgical Lighting System recall (Steris Corporation)
Medical deviceClass IIReported June 24, 2026 · There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads. - Medline convenience kits: HYSTERECTOMY PACK-LF DYNJ20485L recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: C SECTION CDS985505G C SECTION PACK DYNJ68260D ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: ADD-A-CATH ARTERIAL INSERTION ARTNC185 PED SCHOOL AGE... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: BIB AV FISTULA PACK DYNJ58304B CARDIAC MINOR... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: PORT A CATH DYNJ906818A recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: FEMORAL BLOCK TRAY DYNJRA1739B recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: ACL PACK DYNJ64161C ARTHROSCOPY PACK DYNJ47103D ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: DRIVELINE MANAGEMENT KIT EBSI1688 PORT DRESSING... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: 20CM CVC INSERTION KIT ECVC6805B 2L 8.5FR 16CM CVC... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: CMH CENTRAL LINE DRESSING CHANGE KIT EBSI1705A ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Centurion convenience kits: CENTRAL LINE DRESSING SV43 FCP DYNDC2356B DIALYSIS... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: ACD DYNJ904999J ACDF DYNJ907336B DYNJ910821A ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: BASIC EYE DYNJ905154I TUBAL LIGATION CDS CDS760053K recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: DAVINCI MAIN DYNJ908031D recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: WT LAVH PACK DYNJ46609F recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: C-SECTION KIT DYNJ904305J C-SECTION PACK DYNJ69533C recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: DAVINCI DYNJ905836D DAVINCI-LF DYNJ905293I ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kit: SMSC-PELVISCOPY PACK-LF DYNJ0161619M recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kit: recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kit: BHS NEURO DYNJ904900N MEDTRX NEURO PACK DYNJ67267B ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kit: HERNIA REPAIR TOTE DYNJ908337D recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kit: KIT: DRESSING CHANGE PED DYNDC3359 recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kit: IV START KIT W/HUBGUARD DYNDV2662 recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: BASIC DYNJ905869G BASIC PACK DYNJ68484B BIB... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: BREAST IMAGING DYNJT5893 CHOG PLASTICS SYNJ10306A ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: ABD PACK DYNJ81673B BARIATRIC DYNJ902515K ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: DISCECTOMY PACK DYNJ86476B EAR DYNJ81460C ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: BREAST-HERNIA-PORT CDS-LF CDS984853L recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: INPATIENT CENTRAL LN DRSG KIT DYNDC3525 ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: LOOP PACK DYNJ61460C OPEN HEART CDS840150Y ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATH ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - BLOCK TRAY DYNJRA2119A INDWELLING NERVE BLOCK DYNJRA1011A recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline CCI Nerve Block Tray DYNJRA2742 Medline CPNB DYNJRA2716 recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline EBSI Kit EBSI1534 recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Automated Impella Controller recall (Abiomed, Inc.)
Medical deviceClass IReported June 24, 2026 · Potential software error in the Automated Impella Controller ("AIC" ) when used in conjunction with left ventricular Impella devices. - Joolz Recalls Aer2 Car Seat Adapters for Strollers Due to Risk of Serious Injury or Death from Suffocation and Fall Hazards; Violates Mandatory Standard for Infant Sleep Products
Consumer productReported June 18, 2026 · The baby loungers violate the mandatory standard for Infant Sleep Products because the sides are shorter than the minimum side height limit to secure the... - Joolz Recalls Aer2 Car Seat Adapters for Strollers Due to Risk of Serious Injury from Fall Hazard
Consumer productReported June 18, 2026 · The recalled car seat adapters can fail to properly attach to the stroller, which may allow the car seat to fall, posing a risk of serious injury from a fall... - SHEIN Distribution Corporation Recalls Michley Children's Pajamas Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Children's Sleepwear
Consumer productReported June 18, 2026 · The recalled children’s pajamas violate the mandatory flammability standard for children’s sleepwear, posing a risk of serious burn injuries or death. - Bada Boom Fireworks Recalls Pyro Diablo "Diablo Rising" Fireworks Due to Risk of Serious Injury or Death from Explosion and Burn Hazards; Violate Fireworks Ban
Consumer productReported June 18, 2026 · The recalled fireworks violate the ban for aerial fireworks devices intended to produce audible effects because they have a pyrotechnic composition that... - Arizer Solo III Portable Vaporizers Recalled Due to Fire and Burn Hazards; Risk of Serious Injury or Death; Imported by 7111495 Canada
Consumer productReported June 18, 2026 · The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious injury or death to children from burns. - Veseacky Pajama Sets Recalled Due to Risk of Serious Injury Death from Burn Hazard; Violate Mandatory Standards for Children's Sleepwear
Consumer productReported June 18, 2026 · The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious injury or death to children from burns. - Spa Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Arrogantf
Consumer productReported June 18, 2026 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and... - GOPO Toys Recalls Pull String Teething Toys Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys
Consumer productReported June 18, 2026 · The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach... - BABESIDE Doll and Stroller Children's Toys Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Parts Ban; Sold on Amazon by HYBDOLLS
Consumer productReported June 18, 2026 · The recalled toys violate the small parts ban because they are intended for children under three and the small pacifier poses a deadly choking hazard to young... - Individual Unit Label recall (Kettle Cuisine, LLC)
FoodClass IReported June 17, 2026 · Contains undeclared allergen (shrimp). - Merlin" Patient Care System recall (Abbott Medical)
Medical deviceClass IIReported June 17, 2026 · Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command to... - Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE recall (HF Acquisition Co LLC)
Medical deviceClass IIReported June 17, 2026 · Due to incorrect incubation process being performed on product. - Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE recall (HF Acquisition Co LLC)
Medical deviceClass IIReported June 17, 2026 · Due to incorrect incubation process being performed on product. - The Lover Loose-Leaf Tea - Tart Chocolaty Tisane recall (Wild Coast Brew LLC)
FoodClass IIIReported June 17, 2026 · Dry tea blends product containing Ashwagandha root which is an unsafe food additive. - The Creator Loose-Leaf Tea - Ginger Lemongrass Tisane recall (Wild Coast Brew LLC)
FoodClass IIIReported June 17, 2026 · Dry tea blends product containing Ashwagandha root which is an unsafe food additive. - The Shadow Loose-Leaf Tea - Winter Spice Black Tea recall (Wild Coast Brew LLC)
FoodClass IIIReported June 17, 2026 · Dry tea blends product containing Ashwagandha root which is an unsafe food additive. - NEURO NOURISH dietary supplement recall (SENSORY SUPPLEMENT LLC)
FoodClass IIReported June 17, 2026 · Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste. - 1. TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules recall (Total Nutrition Inc)
FoodClass IReported June 17, 2026 · Product may be contaminated with Salmonella. - Park St. Deli Macaroni & Cheese recall (BEF Foods, Inc)
FoodClass IIReported June 17, 2026 · Undeclared allergen (soy lecithin). - BEEKEEPER'S NATURALS Saline Nasal Spray recall (BEEKEEPER'S NATURALS USA INC.)
DrugClass IReported June 17, 2026 · Microbial Contamination of Non-Sterile Products - Budesonide Inhalation Suspension recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIReported June 17, 2026 · Presence of Foreign Substance:This recall has been initiated in response to a product quality complaint reported for black/brown specs and particles within the... - Minocycline Hydrochloride Extended-Release Tablets recall (Ascend Laboratories, LLC)
DrugClass IIReported June 17, 2026 · Failed Dissolution Specifications: An out-of-specification (OOS) result was observed during the 9th month of dissolution test analysis - Gas-X Extra Strength recall (Haleon US Holdings LLC)
DrugClass IReported June 17, 2026 · Chemical Contamination: contamination with a diluted propylene glycol-based coolant from a machine leakage during the packaging process. - Zep recall (Zep Inc)
DrugClass IIReported June 17, 2026 · Microbial contamination of sterile products - Primidone Tablets recall (Amneal Pharmaceuticals, LLC)
DrugClass IIIReported June 17, 2026 · Cross Contamination with Other Products: due to a potential for cross-contamination with Acemetacin API due to an issue at the API manufacturer. - Duloxetine Delayed-Release Capsules recall (Breckenridge Pharmaceutical, Inc.)
DrugClass IIReported June 17, 2026 · CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit - Duloxetine Delayed-Release Capsules recall (Breckenridge Pharmaceutical, Inc.)
DrugClass IIReported June 17, 2026 · CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit - Epinephrine Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIIReported June 17, 2026 · Failed Impurities/Degradations Specifications - DOXOrubin Hydrochloride Liposome injection recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IReported June 17, 2026 · Presence of Particulate matter: Particulate matter identified as glass. - Orca Single Use Air/Water and Suction Valves recall (Boston Scientific Corporation)
Medical deviceClass IIReported June 17, 2026 · Boston Scientific is initiating a medical device removal of Orca Sterile, Single Use Air/Water and Suction Valves due to a higher than anticipated occurrence...