Manufacturer

Mckesson Medical-Surgical Inc. Corporate Office

275 recalls in our database name Mckesson Medical-Surgical Inc. Corporate Office as the manufacturing or recalling firm.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

76–100 of 275

HighFDA (Devices)·Z-1620-2022·2022-08-31
Medical disinfectant recalled due to temperature exposure during storage
McKesson is recalling CaviCide and EnviroCide disinfectants that may have been exposed to excessive temperatures during storage from June to August 2021, potentially reducing their effectiveness.
Product
a. METREX RESEARCH CORP CaviCide1 DISINFECTANT, CLNR CAVICIDE1 1GL (4/CS) METREX, Model Number: 13-5000. b. METREX RESEARCH CORP CaviCide DISINFECTANT, CAVICIDE 8OZ SPRAY MX-1008 METREX Model Number: 13-1008. c. METREX RESEARCH CORP CaviCide DISINFECTANT, CAVICIDE GL MX
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1615-2022·2022-08-31
MedSource IV Start Kit Recalled for Temperature-Related Effectiveness Loss
McKesson is recalling MedSource IV Start kits due to facility temperature excursions that may have compromised product effectiveness. Affected units were received between June and September 2021.
Product
MedSource IV Start kit, 8inch Extension Set IV START KIT, W/SITE LOC/8" EX100/CS Model Number: MS-80047
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1608-2022·2022-08-31
3M Grounding Safety Ring Pads Recalled Due to Temperature Exposure
3M Grounding Safety Ring pads may have been exposed to excessive temperatures during storage, potentially compromising product effectiveness. The recall affects products distributed nationwide that were received between June and September 2021.
Product
3M COMPANY 3M PAD, GROUNDING SAFETY RING Model Number: 9165
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1617-2022·2022-08-31
BD Vacutainer Urine Collection Tubes Recalled for Temperature Exposure
Mckesson Medical-Surgical is recalling BD Vacutainer urine collection tubes and kits due to facility temperature excursions from June to August 2021 that may have compromised preservative effectiveness. All lots distributed between June 1 and September 30, 2021 are affected.
Product
a. BECTON DICKINSON BD Vacutainer C&S Preservative Urine Tube TUBE, URINE COLL PLAS 4ML (100/BX 10BX/CS), Model Number: BD 364951. b. BECTON DICKINSON BD Vacutainer C&S Transfer Straw Kit TRANSFER STRAW KIT, URINE 4ML(50/BX 4BX/CS) Model Number: BD 364953. c. BECTON DICK
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1630-2022·2022-08-31
Centurion Catheter Kits Recalled Due to Temperature Exposure
Mckesson Medical-Surgical is recalling Centurion catheter kits that were exposed to higher temperatures during facility storage prior to delivery, which may have impacted product effectiveness. All units distributed nationwide between June 1 and September 30, 2021 are affected.
Product
CENTURION MEDICAL PRODUCTS, LP Centurion CATH KIT, FML W/LUBE 8FR (50/CS) CNTURN Catalog # CKF105L
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1592-2022·2022-08-31
B. Braun Gravity Mixing Container Recalled for Temperature Exposure
B. Braun EVA Gravity Mixing Container 1000 mL units may have been exposed to higher temperatures during storage prior to delivery, potentially affecting product effectiveness. Units distributed nationwide between June and September 2021 are affected.
Product
B. Braun EVA Gravity Mixing Container 1000 mL Model Number: 2112363
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1623-2022·2022-08-31
Medical device recall for temperature exposure during storage
McKesson Medical-Surgical is recalling multiple medical devices that experienced temperature excursions during storage and transport. Exposure to higher temperatures from June through August 2021 may have reduced product effectiveness.
Product
a. DERMA SCIENCES, INC. NG Strip FASTENER, NASAL TUBE IND WRAP(25/BX), Catalog NG25. b. DERMA SCIENCES, INC. Surgitube BANDAGE, GAUZE #2P 7/8"X50YDS DERSCI Catalog GL-242. c. DERMA SCIENCES, INC. Surgilast TUBE NET SZ3 MED 10YDS/EA HAND, ARM, LEG, FOOT SURGILAST Catalog
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1607-2022·2022-08-31
Chest Drain System Atrium 2100 mL recalled due to temperature exposure
The GETINGE OCEAN Chest Drain System Atrium 2100 mL is being recalled due to facility temperature excursions from June-August 2021 that may have impacted product effectiveness. Affected units were distributed nationwide between June 1 and September 30, 2021.
Product
GETINGE USA SALES LLC OCEAN Chest Drain System Atrium 2100 mL Model Number: 2002-000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1604-2022·2022-08-31
Central Venous Catheter Kits Recalled for Potential Temperature Damage
McKesson Medical-Surgical is recalling Teleflex Arrow Central Venous Catheter Kits due to temperature excursions during storage and shipment. Exposure to higher temperatures may have reduced product effectiveness.
Product
TELEFLEX LLC Arrow Central Venous Catheter Kit 16, 18 Gauge Multi Lumen Model Number:CDC-45703-XP1A (Model Numbers # IPN035619, IPN036437, IPN922677)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1595-2022·2022-08-31
Cadwell Disposable Ground Electrodes Recalled Due to Temperature Exposure
Cadwell Disposable Ground Electrodes may have reduced effectiveness due to facility temperature excursions between June and August 2021. All units distributed nationwide received between June 1 and September 30, 2021 are affected.
Product
Cadwell Disposable Ground Electrodes Grounding Pad 1.25 X 1.75 Inch Dimensions, Disposable Model Number: 302288-000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1586-2022·2022-08-31
ABX PENTRA Creatinine Reagent Recalled Due to Temperature Excursion Exposure
Mckesson Medical-Surgical is recalling ABX PENTRA Creatinine reagent due to facility temperature excursions (June-August 2021) that may have impacted product effectiveness. Affected lots were received nationwide between June 1 and September 30, 2021.
Product
a. ABX PENTRA CREATININE 120CP JAFFE 120/130. Ref: A11A01933. b. Reagent General Chemistry Creatinine Model Number: 1220001933
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1628-2022·2022-08-31
Medical Lubricating Jelly Recalled Due to Temperature Excursions During Storage
Mckesson Medical-Surgical is recalling Fisher Scientific Aseptic Control Lubricating Jelly due to temperature excursions from June–August 2021 that may have reduced product effectiveness.
Product
FISHER SCIENTIFIC Aseptic Control¿ LUBRICATING JELLY PAP TEST 4OZ(12/PK) Catalog #22998006
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1621-2022·2022-08-31
Medical Sponges Recalled for Temperature Exposure During Storage
Mckesson Medical-Surgical is recalling MetriSponge cleaning sponges due to facility temperature excursions that may have compromised product effectiveness during storage and delivery between June and August 2021.
Product
METREX RESEARCH CORP SPONGE, METRISPONGE W/METRIZYME (25/BX 4BX/CS) Model Number: 10-4025
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1585-2022·2022-08-31
Medical Device Etching Solution Recalled for Potential Temperature-Related Effectiveness Loss
ABX Pentra Etching CP solution is recalled due to temperature excursions from June-August 2021 that may have affected product effectiveness. Affected lots were distributed June 1 - September 30, 2021.
Product
HORIBA ABX MEDICAL INC ABX PENTRA ETCHING CP System Fluid ABX Pentra Eching Solution CP For ABX Pentra 400 Clinical Chemistry Analyzer 25 mL. Ref: 1220001769
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1597-2022·2022-08-31
LeadCare II Blood Lead Test Kit Recalled Due to Temperature Storage Issues
81 kits of LeadCare II blood lead test devices were recalled because temperature exposure during storage may have impacted product effectiveness. The affected lots were received between June and September 2021.
Product
MAGELLAN DIAGNOSTICS LeadCare II Blood Lead Test Kit Rapid Test Kit LeadCare II General Chemistry Blood Lead Test Whole Blood Sample 48 Tests Model Number: 70-6762
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1602-2022·2022-08-31
Ultrasound Probe Disinfectant Recalled: Temperature Exposure May Affect Effectiveness
Nanosonics Sonex-HL ultrasound probe disinfectant is recalled due to temperature excursions during storage that may have affected product effectiveness.
Product
NANOSONICS LTD Sonex-HL Ultrasound Probe Disinfectant trophon Sonex-HL 80 mL Bottle For Trophon EPR Disinfection System Model Number: N00037
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1594-2022·2022-08-31
Medical Device Recall: Wetfield Eraser Bipolar Hemostatic due to temperature exposure
McKesson is recalling Wetfield Eraser Bipolar Hemostatic devices that were exposed to elevated facility temperatures from June to August 2021 prior to delivery. This exposure may have impacted the devices' effectiveness.
Product
Wetfield Eraser Bipolar Hemostatic Eraser Wet-Field Eraser 23 Gauge Tapered Model Number: 221265
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1584-2022·2022-08-31
Surgical Hemostatic Matrix Recalled Due to Temperature Exposure During Storage
Mckesson is recalling Ethicon SURGIFLO Hemostatic Matrix Kit due to temperature excursions during storage that may have reduced product effectiveness. Affected units were distributed nationwide between June and September 2021.
Product
Ethicon SURGIFLO Hemostatic Matrix Kit with Thrombin (6/CS) Ref: 2994 Mfg: FERROSAN MEDICAL DEVICES A/S Indicated in surgical procedures (other than ophthalmic) as an adjunct to hemostasis when control of bleeding by ligature or other conventional methods is ineffective
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1593-2022·2022-08-31
Mckesson Ultracell Eye Pledgets Recalled Over Temperature Exposure During Storage
Mckesson Medical-Surgical is recalling Ultracell Eye Pledgets (Model 40825) due to temperature excursions during storage and transportation between June and August 2021 that may have compromised product effectiveness. Affected units were distributed nationwide from June through September 2021.
Product
Ultracell Eye Pledget Ultracell 2 X 6 X 1 mm, Sterile Model Number: 40825
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1583-2022·2022-08-31
McKesson blood coagulation test kits recalled for temperature storage damage
McKesson recalls Coag-Sense blood coagulation test kits nationwide due to facility temperature excursions that may have affected test effectiveness.
Product
a. Rapid Test Kit Coag-Sense Professional Blood Coagulation Test Prothrombin Time Test (PT/INR) Whole Blood Sample 50 Tests-IVD. Part No. 0356-50. b. Coagulation Control Kit Coag-Sense PT / INR Test (Prothrombin Time Test) Low Level / High Level 10 Strips Part No. 03P69-10
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1613-2022·2022-08-31
McKesson GYNECATH H/S Catheter Recalled Due to Temperature Excursions Prior to Delivery
McKesson recalls gynecological catheters that may have been exposed to temperatures higher than intended during storage, potentially affecting product effectiveness. Affected units were received between June and September 2021.
Product
Mckesson GYNECATH H/S CATHETER 5FR (10/CS) Model Number: 11-19610
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1590-2022·2022-08-31
Alcon Contact Lens Solutions Recalled for Temperature Exposure During Storage and Transit
Multiple Alcon contact lens solutions were recalled due to facility temperature excursions during storage and transit that may have reduced product effectiveness. Affected products include Clear Care and Opti Free Replenish solutions distributed nationwide between June and September 2021.
Product
a. Alcon Clear Care Contact Lens Solution Clear Care 12 oz. Solution, Model Number: 65035820, Model Number: USSCupA-12BUP300. b. Alcon Contact Lens Solution Opti Free Replenish 4 oz. Solution Model Number: 00065035604 Model Number: USSCupA-12BUP300. c. Alcon Contact L
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1632-2022·2022-08-31
Morrison Medical OB Kit Recalled Due to Temperature Excursion During Storage
Mckesson is recalling Morrison Medical OB Kits because facility temperature excursions may have reduced product effectiveness. All lots received between June 1 and September 30, 2021 are affected.
Product
MORRISON MEDICAL Morrison Medical OB KIT, HARD PK SEALED W/CARDBOARD BX MORMED Catalog #0967NL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1625-2022·2022-08-31
Surgical ophthalmic wicks recalled for potential effectiveness loss
McKesson Medical-Surgical Inc. is recalling Beaver-Visitec Ultracell surgical wicks due to facility temperature excursions during storage. Temperature exposure may have impacted product effectiveness, affecting units distributed nationwide between June and September 2021.
Product
BEAVER-VISITEC INTERNATIONAL, INC. Ultracell WICK, FENSTD PED 7MMX20MM(10/BX) BVRVIS Catalog #30316-C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1606-2022·2022-08-31
Alere Fertility Test Pregnancy Test Kits Recalled Due to Temperature Damage
Alere Fertility Test pregnancy test kits distributed in the US have been recalled because temperature excursions during storage may have reduced product effectiveness. All lots received between June 1 and September 30, 2021 are affected.
Product
a. ABBOTT RAPID DX N AMERICA LLC Alere Rapid Test Kit Alere Fertility Test hCG Pregnancy Test Urine Sample 30 Tests, Model Number: 92210. b. ABBOTT RAPID DX N AMERICA LLC Alere Rapid Test Kit Alere hCG Dipstick Fertility Test hCG Pregnancy Test Urine Sample 50 Tests Model Num
Category
Medical Device
Distribution
Distributed nationwide