Recalls in Texas (page 26)
4158 recalls.
- RAW FARM ORIGINAL RAW CHEDDAR 80 OZ [BULK ITEM] recall (Raw Farm LLC)
FoodClass IReported May 13, 2026 · Multi-state outbreak of E. coli O157:H7. - RAW FARM SHREDDED RAW CHEDDAR 80 OZ [BULK ITEM] recall (Raw Farm LLC)
FoodClass IReported May 13, 2026 · Multi-state outbreak of E. coli O157:H7. - RAW FARM RAW CHEDDAR SIMPLY SHREDDED Original MADE WITH: WHOLE RAW MILK TRULY RAW -... recall (Raw Farm LLC)
FoodClass IReported May 13, 2026 · Multi-state outbreak of E. coli O157:H7. - RAW FARM RAW CHEDDAR Jalapeno NEVER WARMED ABOVE 102F recall (Raw Farm LLC)
FoodClass IReported May 13, 2026 · Multi-state outbreak of E. coli O157:H7. - RAW FARM RAW CHEDDAR Original NEVER WARMED ABOVE 102F recall (Raw Farm LLC)
FoodClass IReported May 13, 2026 · Multi-state outbreak of E. coli O157:H7. - Good & Gather Fresh from Our Deli. Sesame Teriyaki Chicken with Rice. Net Wt 18.0 oz recall (Target Corporation)
FoodClass IIReported May 13, 2026 · Undeclared allergens (sesame and soy) - french broad CHOCOLATE bette's bake sale recall (French Broad Chocolate Factory)
FoodClass IReported May 13, 2026 · Undeclared nut allergen (walnut) due to mislabeling. The product's printed tasting guide incorrectly identifies the Walnut Fudge and Peach Cobbler flavor... - Hatch Green Chile Creamed Honey 671333101339 * These product labels may also say ... recall (Walker Honey Co)
FoodClass IIReported May 13, 2026 · Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic. - Darkside of the Hive Creamed Honey/Salted Chocolate Creamed Honey 671333101414 *These... recall (Walker Honey Co)
FoodClass IIReported May 13, 2026 · Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic. - Natural Creamed Honey recall (Walker Honey Co)
FoodClass IIReported May 13, 2026 · Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic. - Lemon Creamed Honey recall (Walker Honey Co)
FoodClass IIReported May 13, 2026 · Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic. - Hatch Creamed Honey 671333101339 * These product labels may also say Whipped Honey ... recall (Walker Honey Co)
FoodClass IIReported May 13, 2026 · Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic. - Dark Pecan Creamed Honey/Pecan Creamed Honey 671333101407 * These product labels may... recall (Walker Honey Co)
FoodClass IIReported May 13, 2026 · Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic. - Cinnamon Creamed Honey 671333101360 * These product labels may also say Whipped Honey... recall (Walker Honey Co)
FoodClass IIReported May 13, 2026 · Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic. - Blackberry Creamed Honey 671333101308 * These product labels may also say Whipped... recall (Walker Honey Co)
FoodClass IIReported May 13, 2026 · Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic. - Raspberry Creamed Honey 671333101322 ¿ These product labels may also say Whipped... recall (Walker Honey Co)
FoodClass IIReported May 13, 2026 · Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic. - Fain s Blackberry Honey Spread recall (Walker Honey Co)
FoodClass IIReported May 13, 2026 · Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic. - SunRidge Farms Organic SUNSET SOUP MIX CERTIFIED ORGANIC BY QAI recall (Falcon Trading Co., Inc.)
FoodClass IIIReported May 13, 2026 · Potential contamination with pesticides, haloxyfop and thiamethoxam - SunRidge Farms Organic CHILI BEAN BLEND CERTIFIED ORGANIC BY QAI recall (Falcon Trading Co., Inc.)
FoodClass IIIReported May 13, 2026 · Potential contamination with pesticides, haloxyfop and thiamethoxam - SunRidge Farms Organic Black Beans CERTIFIED ORGANIC BY QAI recall (Falcon Trading Co., Inc.)
FoodClass IIIReported May 13, 2026 · Potential contamination with pesticides, haloxyfop and thiamethoxam - MILK-N-EGG MIX recall (Griffith Foods Inc.)
FoodClass IReported May 13, 2026 · Potential Salmonella contamination. The firm was notified from their supplier that the nonfat dry milk may be contaminated with Salmonella. - MILK WASH recall (Griffith Foods Inc.)
FoodClass IReported May 13, 2026 · Potential Salmonella contamination. The firm was notified from their supplier that the nonfat dry milk may be contaminated with Salmonella. - Costco Service Deli Department 63 MEATLOAF SEASONING MORE FLV Pack Size: 4-5lb. Bags... recall (Griffith Foods Inc.)
FoodClass IReported May 13, 2026 · Potential Salmonella contamination. The firm was notified from their supplier that the nonfat dry milk may be contaminated with Salmonella. - Biofire Spotfire Respiratory/Sore Throat Panel REF: 423485 recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported May 13, 2026 · Respiratory/sore throat panel test may result in false negative results and control failures. - BioFire Joint Infection recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported May 13, 2026 · Contamination to in-vitro diagnostic test may result in false positives. - LIFEPAK 15 recall (Physio-Control, Inc.)
Medical deviceClass IIReported May 13, 2026 · Some defibrillators serviced between July 2023 through November 2025 were serviced without objective evidence that a Performance Inspection Procedure (PIP) was... - ERBEFLO 2 recall (Erbe Medical, LLC)
Medical deviceClass IIReported May 13, 2026 · Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible... - ERBEFLO CleverCap: Hybrid Tubing/Cap Set for Olympus Scopes recall (Erbe Medical, LLC)
Medical deviceClass IIReported May 13, 2026 · Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible... - ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources recall (Erbe Medical, LLC)
Medical deviceClass IIReported May 13, 2026 · Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible... - Brand Name: Spacelabs Ultraview SL Command Module Product Name: SL Command Module ... recall (Spacelabs Healthcare, Inc.)
Medical deviceClass IIReported May 13, 2026 · Due to a manufacturing issue (i.e. malfunctioning of electrical Leakage tester). - Prodisc C SK U.S. IMPLANT EXTRA LARGE 6MM. Model Number: PDSXL6. Total cervical... recall (Centinel Spine, Inc.)
Medical deviceClass IIReported May 13, 2026 · Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was... - Prodisc C SK U.S. IMPLANT EXTRA LARGE 5MM. Model: PDSXL5 Total cervical disc... recall (Centinel Spine, Inc.)
Medical deviceClass IIReported May 13, 2026 · Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was... - Brand Name: Da Vinci X and Da Vinci Xi Product Name: da Vinci X recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported May 13, 2026 · Due to manipulator containing screws with in the arm sub-assembly that my be susceptible to breaking. - Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard SAMMC ANGIOGRAPHY kit. Model Numbers: SAMM066-15. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard PERC TRAY kit. Model Numbers: SLPC34-01 recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard NEURO IR PERIPHERAL recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard HEART CATH recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CATH LAB kit. Model Number: SACL75-01. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CATH LAB kit. Model Number: SACL75AM. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04 recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05 recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06 recall (Intuitive Surgical, Inc.)
Medical deviceClass IReported May 13, 2026 · Reloads for curved-tipped stapler may potentially produce an incomplete staple line. - Woodstock Organic Shelled Edamame 10 oz. and 48 oz. recall (Green Organic Vegetables)
FoodClass IIReported May 13, 2026 · Foreign object: metal pieces - Lactated Ringer's Injection USP recall (B BRAUN MEDICAL INC)
DrugClass IReported May 13, 2026 · Presence of Particulate Matter. - NAPROXEN ORAL SUSPENSION recall (Acella Pharmaceuticals, LLC)
DrugClass IIReported May 13, 2026 · Chemical contamination; presence of lead and lithium above specification - Duloxetine Delayed-Release Capsules USP recall (Breckenridge Pharmaceutical, Inc.)
DrugClass IIReported May 13, 2026 · CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit - Enalapril Maleate Tablets recall (JB Chemicals and Pharmaceuticals Ltd)
DrugClass IIReported May 13, 2026 · Failed Impurities/Degradation Specifications:Out of specification result occurred in Organic Impurities Test - Octreotide Acetate for Injectable Suspension recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported May 13, 2026 · Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract... - BD PurPrep recall (CareFusion 213, LLC)
DrugClass IIReported May 13, 2026 · Lack of assurance of Sterility: potential product contamination - BD PurPrep recall (CareFusion 213, LLC)
DrugClass IIReported May 13, 2026 · Lack of assurance of Sterility: potential product contamination - Duloxetine Delayed-Release Capsules recall (Ajanta Pharma Ltd.)
DrugClass IIReported May 13, 2026 · CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability... - Duloxetine Delayed-Release Capsules recall (Ajanta Pharma Ltd.)
DrugClass IIReported May 13, 2026 · CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability... - Duloxetine Delayed-Release Capsules recall (Ajanta Pharma Ltd.)
DrugClass IIReported May 13, 2026 · CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability... - DELFLEX recall (Fresenius Medical Care Holdings, Inc.)
DrugClass IIReported May 13, 2026 · Lack of Assurance of Sterility: Potential leaks from perforations in bags. - DELFLEX recall (Fresenius Medical Care Holdings, Inc.)
DrugClass IIReported May 13, 2026 · Lack of Assurance of Sterility: Potential leaks from perforations in bags. - busPIRone Hydrochloride Tablets recall (Unichem Pharmaceuticals USA Inc.)
DrugClass IIIReported May 13, 2026 · Subpotent drug - ZENBONE recall (Orthorebirth Co Ltd)
Medical deviceClass IIReported May 13, 2026 · Resorbable bone void filler falls outside standard specifications. - BioCera Fibers recall (Orthorebirth Co Ltd)
Medical deviceClass IIReported May 13, 2026 · Resorbable bone void filler falls outside standard specifications. - Medline Surgical Packs: 1) PACK recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - See complete list in RES recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Surgical Drapes: 1) SHEET recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ARTHROSCOPY CDS recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT UROLOGY SLING recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) LVAD DRIVELINE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DRAPE PACK recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DRAPE PACK-CHOICE recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT GENERAL CLOSURE recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BURN PACK recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) WMC I D PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) PICC CATHETER INSERTION TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BAPTIST FLOYD ENDO GI KIT recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BASIC NERVE BLOCK TRAY W/LINEN recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT STC TRACHEOSTOMY recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - See RES for complete list. Medline Convenience Kits: 1) SPINAL CDS recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT OPHTHALMIC RUPTURE GLOBE recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BAP NORTH ROBOTIC SURGERY CDS recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) HYSTEROSCOPY recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) C-SECTION PACK recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - See full list in RES recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) OB KIT recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) NEURO SHUNT- CODMAN recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) CHEST TUBE INSERTION TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ADMIT KIT recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) PPE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) CENTRAL LINE UNIVERSAL INSERTI recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) CVC PACK recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - See RES for complete list. Medline Convenience Kits: 1) DRAWER 6-IV FLUIDS GLOVES recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) LITHOTOMY PACK recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - See RES for complete list. Medline Convenience Kits: 1) PLASTIC BIN W/MISC KITS recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - See RES for complete list. Medline Convenience Kits: 1) MAJOR LAPAROTOMY CDS recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - See RES for full list. Medline Convenience Kits: 1) CHP COCHLEAR SUPPLEMENT CDS recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DYNDA3003 recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT SURG ONC EXCISION BREAST recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) PICC LINE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - See RES for complete list. Medline Convenience Kits: 1) OPEN HEART CDS recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ANGIO PROCEDURE PACK recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ANGIO PROCEDURE PACK recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated...