Recalls in New York (page 19)
4155 recalls.
- Al Yaman Halawa Extra Pistachio 907g recall (GREENWORLD FOOD EXPRESS (USA) LLC)
FoodClass IReported June 24, 2026 · Product may be contaminated with Salmonella - Great Value Hawaiian Roll 4pk recall (United States Bakery)
FoodClass IIReported June 24, 2026 · Firm observed oily and sticky substance on direct food contact surface packaging of finished product. - Brand Name: HeartMate Product Name: HM 11V Li-ion Backup Battery recall (Thoratec LLC)
Medical deviceClass IIReported June 24, 2026 · Due to 11 volt Backup Battery failures. - Brand Name: HeartMate Product Name: HeartMate 3" System Controller Model/Catalog... recall (Thoratec LLC)
Medical deviceClass IIReported June 24, 2026 · Due to 11 volt Backup Battery failures. - Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System recall (Thoratec LLC)
Medical deviceClass IIReported June 24, 2026 · Due to 11 volt Backup Battery failures. - Splashwire Hydrophilic Guide Wire: REF: MSWSTDA35150 UDI-DI codes: 00884450529645 ... recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported June 24, 2026 · Due to unsealed portions of pouches. - BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta"... recall (BD SWITZERLAND SARL)
Medical deviceClass IIReported June 24, 2026 · Due to stopcock issues when using the plastic luer-lok syringe, the connection at the Port C may over thread or continue to spin rather than tightening... - Product Name: STAAR ICL Calculation Software Software Version: Version 8.00 Product... recall (Staar Surgical AG)
Medical deviceClass IIReported June 24, 2026 · Due to a software coding issues for calculating the implant orientation diagram printout for the implantation for toric implantable collamer lenses. - 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. - Description/REF: RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-1A recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: CVC KIT: 16 GA X 8IN/AK-04210 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PICC ACCESS TRAY/ASK-04001-CG1 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: MIDLINE CATHETER KIT: 3 FR X 20 CM/CDC-02031-MK1A recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PSI KIT: 7 FR X 4 IN/ASK-09701-UP recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ACCESS TRAY/ASK-04001-MC3 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: RA CATH KIT: 20 GA X 1-3/4IN/AK-04020-SPC recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: SAC KIT: 18 GA X 12CM W BIO/SAC-01218-B recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: SPINAL ANESTHESIA KIT/ASA-24090-SB recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 20 CM/AK-15122-F recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PI MIDLINE 2L: 5FR X 20CM/CDC-32052-MPKC recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PARACENTESIS KIT/ASK-00376-JHH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ACCESS TRAY/GU-04020 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ACCESS TRAY/ASK-04001-JHH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PACING/PSI KIT: 5 FR 2L/ASK-07155-MGU recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: DRAINAGE KIT/AK-01600 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-12122-F recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PI JACC KIT: 2L 5.5 FR X 15 CM CG+/ASK-41552-LTAC recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PI PICC: 3: 6FR x 55CM w CHG/ DLX-35563-HPKC recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ARTERIAL LINE KIT: SL 20 GA X 5 IN/ASK-04510-MM6 RA CATH KIT: 20 GA X... recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: CVC/PSI KIT: 2 LUMEN 8 FR X 6 IN/ASK-42802-PLH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PNHS2 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: AHDC KIT: 3-L 12 FR X 16 CM/AK-12123-PCDC recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: HEMODIALYSIS KIT: 2-LUMEN 8 FR X 11 CM/AK-11802-F recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: HEMODIALYSIS KIT: 2L 14 FR X 20 CM AGB CDC-25142-X1A recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05502-VM1 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PI AGBA PICC KIT: 3L 6 FR X 40 CM W/VPS/ASK-44063-NS AGBA... recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PSI KIT: 7 FR X 4IN ANTIMICROBIAL/ASK-09701-UMH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: RA CATH KIT: 20 GA X 1 3/4 IN/TJ-04020-1 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: AGBA PICC G4 Stylet: 3L 6FR x 55CM BP/DLX-45563-VPSB recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PACING PSI KIT: 6 FR/AI-06210-KS recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: BIOPSY SYSTEM COMPREHENSIVE KIT/ASK-09458-AH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ACCESS TRAY/ASK-04001-SUH-S recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - PARACENTESIS KIT recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Cura Hongos recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Rapidol recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Lil Drug Store recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Circle K recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Lucky Super Soft recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Lucky Super Soft recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Chlorthalidone Tablets recall (Inventia Healthcare Limited)
DrugClass IIReported June 24, 2026 · Failed Dissolution Specifications - Focalin XR recall (Sandoz Inc)
DrugClass IIIReported June 24, 2026 · Labeling: Incorrect or Missing Lot and/or Exp Date - safco SensiCaine-Ultra recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - PureLife recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - Dental City TOPICAL ANESTHETIC GEL recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - Burkhart topical anesthetic gel recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - DHP Topical Anesthetic Gel recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - Quala Dental Products recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - Pearson Quality Topical Anesthetic Gel recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - Buprenorphine HCl recall (Par Health USA, LLC)
DrugClass IIReported June 24, 2026 · Crystallization; identified as Buprenorphine free base - Aripiprazole Tablets USP recall (Ajanta Pharma USA Inc)
DrugClass IIReported June 24, 2026 · Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg. - Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride recall (IntegraDose Compounding Services LLC)
DrugClass IIReported June 24, 2026 · Subpotent Drug - VistaPharm recall (PAI Holdings LLC)
DrugClass IIReported June 24, 2026 · Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023 - VistaPharm recall (PAI Holdings LLC)
DrugClass IIReported June 24, 2026 · Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023 - VistaPharm recall (PAI Holdings LLC)
DrugClass IIReported June 24, 2026 · Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023 - VistaPharm recall (PAI Holdings LLC)
DrugClass IIReported June 24, 2026 · Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023 - Alyacen 7/7/7 recall (Glenmark Pharmaceuticals Inc., USA)
DrugClass IIReported June 24, 2026 · Failed Impurities/Degradation Specifications: This recall is being initiated due to out-of-specification results total impurities. - Brand Name: Inspire Medical Systems recall (Inspire Medical Systems Inc.)
Medical deviceClass IIReported June 24, 2026 · Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation of a... - Brand Name: Inspire Medical Systems recall (Inspire Medical Systems Inc.)
Medical deviceClass IIReported June 24, 2026 · Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation of a... - MEDLINE Medical Procedure Kits labeled as: 1) CRANI 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) RETINA LAC/USC CDS 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: KIT URO ROBOT CYSTECTOMY 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 CLOVIS HYSTEROSCOPY 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) D AND C 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 BASIC GYN 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: PELVIC LAP 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: 1) BR L&D 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: 1) CAROTID NEURO 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: NURSING KIT 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: DR FERNANDEZ 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 BIOBURDEN TEST KIT 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) CV DRAPING/BASIN 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) KIT UROLOGY URETHROPLASTY 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: TONSIL PACK CATH 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) CHEST EXPLORATION ECMO 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: 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...