Recalls in May 2026
579 recalls.
- Boner Bears CHOCOLATE recall (JXK Enterprises, Inc.)
FoodClass IReported November 4, 2026 · JXK Enterprises, Inc is voluntarily recalling Boner Bears Chocolate, Lot #BB21125, after being notified that FDA laboratory analysis confirmed the presence of... - Coco G's Courmet Flaming Cheddar Hots recall (Coco G's Snack Foods, Inc.)
FoodClass IReported October 7, 2026 · Potential Salmonella contamination. - nGenuity Patient Monitor with Capnography recall (Criticare Technologies, Inc.)
Medical deviceClass IIReported September 30, 2026 · Complaint trend where "Checkline Error" alarm presents at device setup, rendering the CO2 monitoring function inoperable. May result in procedure delay. - IV Sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - IV Sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - IV Sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - IV Sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - Oncology sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - Oncology sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - IV Non-Dedicated Gravity Administration Sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - Plum administration sets recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - Halyard medical convenience kits labeled as: 1) A-P PACK - 205936 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 9, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - 1) NEURO recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 9, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - Halyard medical convenience kits labeled as: 1) ENT recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 9, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - American Contract Systems medical procedure kits and trays labeled as: 1) ANTERIOR... recall (American Contract Systems Inc)
Medical deviceClass IIReported August 26, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - American Contract Systems medical procedure kits and trays labeled as: 1) CRANI... recall (American Contract Systems Inc)
Medical deviceClass IIReported August 26, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 ... recall (Covidien, LLC)
Medical deviceClass IIReported August 26, 2026 · The system's 24-hour usage limit results in catheters incorrectly flagged as expired, making them unavailable for clinical procedures. - Dark Chocolate Coconut Almond Bites recall (Bazzini LLC)
FoodClass IReported August 19, 2026 · Undeclared peanuts - ProNephro AKI recall (Bioporto Diagnostics A/S)
Medical deviceClass IIReported August 19, 2026 · The use of a non-validated rework process for assay reagents which could lead to missed diagnosis of renal disease, inappropriate treatment decisions, or... - GORE VIABIL Short Wire Biliary Endoprosthesis recall (W L Gore & Associates, Inc.)
Medical deviceClass IIReported August 19, 2026 · 10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes... - GORE VIABIL Short Wire Biliary Endoprosthesis recall (W L Gore & Associates, Inc.)
Medical deviceClass IIReported August 19, 2026 · 10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes... - GEM Premier 5000 PAK Part Numbers: 00055360010 00055360011 00055407504 ... recall (Instrumentation Laboratory)
Medical deviceClass IIReported August 12, 2026 · The active ingredient concentration in the lysing bag solution of specific GEM Premier 5000 lots did not meet established manufacturing specifications. The... - GEM Premier 7000 with iQM3 Part Numbers: 00077407508 00077407510 00077415004 ... recall (Instrumentation Laboratory)
Medical deviceClass IIReported August 12, 2026 · The active ingredient concentration in the lysing bag solution of specific GEM Premier 7000 with iQM3 PAK lots did not meet established manufacturing... - Brand Name: U2 Total Knee System Product Name: Femoral valgus offset adaptor recall (United Orthopedic Corp.)
Medical deviceClass IIReported August 12, 2026 · Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail. - Brand Name: U2 Total Knee System Product Name: Femoral valgus adaptor recall (United Orthopedic Corp.)
Medical deviceClass IIReported August 12, 2026 · Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail. - Brand Name: USTAR II Knee System Product Name: Hinge Box Trial recall (United Orthopedic Corp.)
Medical deviceClass IIReported August 12, 2026 · Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail. - Brand Name: U2 Total Knee System Product Name: PSA Box Trial recall (United Orthopedic Corp.)
Medical deviceClass IIReported August 12, 2026 · Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail. - Anti-Torque recall (Innovasis, Inc)
Medical deviceClass IIReported August 12, 2026 · Pedicle screw system intended to provide immobilization/stabilization of spinal segments as adjunct to thoracic/lumbar/sacral spine fusion may have anti-torque... - Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear... recall (Medical Action Industries, Inc. 306)
Medical deviceClass IIReported August 12, 2026 · Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal. - DQ Chocolate Reduced Fat Ice Cream Mix recall (Galliker Dairy Co, Inc.)
FoodClass IIReported August 5, 2026 · Foreign material found in product (identified as metal shavings) - Brand Name: GEM Premier 5000 Product Name: GEM Premier 5000 Model/Catalog Number:... recall (Instrumentation Laboratory)
Medical deviceClass IIReported August 5, 2026 · Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID. - Brand Name: GEM Premier 5000 Product Name: GEM Premier 5000 Model/Catalog Number:... recall (Instrumentation Laboratory)
Medical deviceClass IIReported August 5, 2026 · Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID. - Brand Name: GEM Premier 5000 Product Name: GEM Premier 5000 Model/Catalog Number:... recall (Instrumentation Laboratory)
Medical deviceClass IIReported August 5, 2026 · Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID. - Brand Name: GEM Premier 5000 Product Name: GEM Premier 5000 Model/Catalog Number:... recall (Instrumentation Laboratory)
Medical deviceClass IIReported August 5, 2026 · Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID. - Brand Name: GEM Premier 7000 with iQM3 Product Name: GEM Premier 7000 with iQM3... recall (Instrumentation Laboratory)
Medical deviceClass IIReported August 5, 2026 · Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID. - GEM Premier 5000 with IQM2 Model/Catalog Number: 00024019255 and GEM Premier 7000... recall (Instrumentation Laboratory)
Medical deviceClass IIReported August 5, 2026 · Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID. - Pack Angiography NCMC 3/Cs BANNER recall (Medical Action Industries, Inc. 306)
Medical deviceClass IReported August 5, 2026 · Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be... - Power Over Fiber Base Module recall (Terex Utilities)
Medical deviceClass IIReported August 5, 2026 · Device not certified - no laser product report was filed with CDRH prior to distribution. Product label incorrectly states device is "Class IV", although... - Flexible Hystero-Fiberscope Kits REF: 11264BBU1 recall (Karl Storz Endoscopy)
Medical deviceClass IIReported July 29, 2026 · Flexible hysteroscopes indicated for use during diagnostic and operative hysteroscopic procedures may contain an expired single use endoscopic seal for... - SafeOp Patient Interface recall (Alphatec Spine, Inc.)
Medical deviceClass IIReported July 29, 2026 · Intraoperative neuromonitoring device, due to a software issue, may experience loss or interruption of triggered electromyography (tEMG) functionality during... - Emano Flow with software version v2.0.0 GS1 GTIN code: 199874903484 Emano Flow is... recall (Emano Metrics, Inc.)
Medical deviceClass IIReported July 29, 2026 · 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... - Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. ... recall (AVID Medical, Inc.)
Medical deviceClass IIReported July 29, 2026 · Defects in the silicone seal, which may result in "doming" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or leakage. - 3mensio Workstation recall (PIE Medical Imaging B.V.)
Medical deviceClass IIReported July 29, 2026 · User measurement value reported by diagnostic bioimaging software intended to measure/visualize cardiovascular structures may be larger (0.8% to 34.4%) than... - Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit. recall (AVID Medical, Inc.)
Medical deviceClass IIReported July 29, 2026 · Incorrect concentration of Betadine solution contained within certain AVID convenience kits. - SeaSpine Polyaxial Head REF Number: 41-3010 recall (SEASPINE ORTHOPEDICS CORPORATION)
Medical deviceClass IIReported July 29, 2026 · Due to manufacturing error, polyaxial head may popoff from the screw intraoperatively following insertion. - Ruby recall (GELLERT GLOBAL GROUP)
FoodClass IIReported July 22, 2026 · Foreign material (Glass) was found in the product. - Ice Pop recall (D'Dioses Fruit Pops, Inc.)
FoodClass IReported July 22, 2026 · May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. - Ice Pop recall (D'Dioses Fruit Pops, Inc.)
FoodClass IReported July 22, 2026 · May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. - Ice Pop recall (D'Dioses Fruit Pops, Inc.)
FoodClass IReported July 22, 2026 · May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. - Ice Pop recall (D'Dioses Fruit Pops, Inc.)
FoodClass IReported July 22, 2026 · May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. - Ice Pop recall (D'Dioses Fruit Pops, Inc.)
FoodClass IReported July 22, 2026 · May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. - Ice Pop recall (D'Dioses Fruit Pops, Inc.)
FoodClass IReported July 22, 2026 · May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. - Ice Pop recall (D'Dioses Fruit Pops, Inc.)
FoodClass IReported July 22, 2026 · May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. - Ice Pop recall (D'Dioses Fruit Pops, Inc.)
FoodClass IReported July 22, 2026 · May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. - Ice Pop recall (D'Dioses Fruit Pops, Inc.)
FoodClass IReported July 22, 2026 · May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. - Ice Pop recall (D'Dioses Fruit Pops, Inc.)
FoodClass IReported July 22, 2026 · May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. - Ice Pop recall (D'Dioses Fruit Pops, Inc.)
FoodClass IReported July 22, 2026 · May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. - Ice Pop recall (D'Dioses Fruit Pops, Inc.)
FoodClass IReported July 22, 2026 · May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. - Ice Pop recall (D'Dioses Fruit Pops, Inc.)
FoodClass IReported July 22, 2026 · May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. - Ice Pop recall (D'Dioses Fruit Pops, Inc.)
FoodClass IReported July 22, 2026 · May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. - Ice Pop recall (D'Dioses Fruit Pops, Inc.)
FoodClass IReported July 22, 2026 · May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. - Ice Pop recall (D'Dioses Fruit Pops, Inc.)
FoodClass IReported July 22, 2026 · May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. - functional formularies NOURISH ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA... recall (Nutricia North America)
FoodClass IIReported July 22, 2026 · 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... - functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE... recall (Nutricia North America)
FoodClass IIReported July 22, 2026 · 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... - Medtronic Bio-Medicus Adult Cannula Kit recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 22, 2026 · Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood. - Medtronic DLP One-Piece Pediatric Arterial Cannula recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 22, 2026 · Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood. - Papablic Replacement Brush Heads. Model Number: PAPA317AA. recall (Papablic Inc)
Medical deviceClass IIReported July 22, 2026 · Potential for brush heads to break. - Papablic Replacement Brush Heads. Model Number: Papablic18B recall (Papablic Inc)
Medical deviceClass IIReported July 22, 2026 · Potential for brush heads to break. - Olympus Glass Body for 194 Ellik Evacuator. Model Number: 190A. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Olympus Ellik Evacuator Includes Glass Body recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Olympus Toomey Evacuator 50cc with Adaptor. Model Number: 188A. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Olympus Toomey Evacuator 30cc with Adaptor. Model Number: 188. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Wise Onion Rings recall (Wise Foods Inc)
FoodClass IIReported July 15, 2026 · The product contains undeclared Yellow 5 and 6, Blue 1, and unapproved Red 3. - Vanilla Dessert Shells recall (Specialty Bakers, LLC)
FoodClass IIReported July 15, 2026 · Undeclared Allergen (Soy) - Clomiphene Citrate USP Active Pharmaceutical Ingredient recall (Shimoga Chemicals)
DrugClass IIReported July 15, 2026 · cGMP deviations - Drogueria San Juan Puerto Rico Isopropyl Alcohol 70% recall (Gasco Industrial Corp.)
DrugClass IIReported July 15, 2026 · Subpotent drug - Drogueria San Juan Puerto Rico Isopropyl Alcohol 70% recall (Gasco Industrial Corp.)
DrugClass IIReported July 15, 2026 · Subpotent drug - Drogueria San Juan Puerto Rico Isopropyl Alcohol 70% recall (Gasco Industrial Corp.)
DrugClass IIReported July 15, 2026 · Subpotent drug - Gasco Isopropyl Alcohol 70% recall (Gasco Industrial Corp.)
DrugClass IIReported July 15, 2026 · Subpotent drug - Gasco Isopropyl Alcohol 70% recall (Gasco Industrial Corp.)
DrugClass IIReported July 15, 2026 · Subpotent drug - Gasco Isopropyl Alcohol 70% recall (Gasco Industrial Corp.)
DrugClass IIReported July 15, 2026 · Subpotent drug - TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia... recall (Think Surgical, Inc.)
Medical deviceClass IIReported July 15, 2026 · Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array. - GSP Neonatal GALT Kit. Product Codes: 3303-001U recall (WALLAC OY)
Medical deviceClass IIReported July 15, 2026 · Reduction in the on-board stability of the GSP GALT assay. This may increase the likelihood of run-QC failures and consequently delay the reporting of patient... - 5008X Blood Tubing Set recall (Fresenius Medical Care Holdings, Inc.)
Medical deviceClass IIReported July 15, 2026 · Potential for Online Port Errors due to connection issues when connecting the SafeLine of the 5008X CAREset to the substitution fluid port of the 5008X... - MiniMed 780G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported July 15, 2026 · A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and... - Medline Convenience Kits: 1) OPEN HEART PEDS PACK recall (Medline Industries, LP)
Medical deviceClass IIReported July 15, 2026 · 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... - Medline Convenience Kits: 1) OPEN HEART PEDS PACK recall (Medline Industries, LP)
Medical deviceClass IIReported July 15, 2026 · 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... - Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF recall (Medline Industries, LP)
Medical deviceClass IIReported July 15, 2026 · 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... - MOGO PURE MORINGA OLEIFERA CAPSULES recall (MOGO Moringa LLC)
FoodClass IReported July 8, 2026 · Product may be contaminated with Salmonella Typhimurium - GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers recall (W L Gore & Associates, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to catheter separation - Solar GI System recall (Laborie Medical Technologies Corp)
Medical deviceClass IIReported July 8, 2026 · Under extended clinical use conditions (e.g., long duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's... - 4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108563 4382A SOFT... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188770 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741035258 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236129... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138478 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by...