Manufacturer

Mckesson Medical-Surgical Inc. Corporate Office

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

What the numbers show

Total: 276
Critical: 0
Severe: 0
Most recent: 2025-08-27

Of the 276 recalls from Mckesson Medical-Surgical Inc. Corporate Office we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

Which agencies issued them

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.

101–125 of 276

HighFDA (Devices)·Z-1601-2022·2022-08-31
McKesson Colorectal Cancer Screening Tests Recalled Due to Temperature Exposure
McKesson Medical-Surgical is recalling MMS - IMMUNOSTICS INC colorectal cancer screening test kits due to facility temperature excursions that may have reduced product effectiveness. The recall affects lots distributed between June and September 2021.
Product
a. MMS - IMMUNOSTICS INC McKesson Rapid Test Kit Consult Colorectal Cancer Screening Fecal Occult Blood Test (iFOB or FIT) Stool Sample 25 Tests, Model Number: 4487. b. MMS - IMMUNOSTICS INC McKesson Rapid Test Kit McKesson Consult Colorectal Cancer Screening Fecal Occult Blo
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-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
ModerateFDA (Devices)·Z-1619-2022·2022-08-31
McKesson Medefil Normal Saline IV Flush Syringes Recalled for Temperature Exposure
McKesson is recalling Medefil Normal Saline IV Flush Syringes (Models MIS-1130 and 191-MIS-1130) due to facility temperature excursions between June and August 2021. Products received through September 30, 2021 may have impaired effectiveness from temperature exposure prior to delivery.
Product
a. Medefil Normal Saline IV Flush Syringe NORMAL SALINE FLUSH, SYR 10ML/12ML (60/BX 16BX/CS), Model Number: MIS-1130. b. MEDEFIL INC McKesson SALINE IV FLUSH, SYR NORMAL 10ML/12ML .9% (60/BX 16BX/CS) Model Number: 191-MIS-1130.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1612-2022·2022-08-31
Fischer Cone Biopsy Excisor recalled for potential temperature damage
McKesson is recalling Fischer Cone Biopsy Excisor Model 900-157 units because temperature excursions during storage may have compromised product effectiveness.
Product
Fischer Cone Biopsy Excisor EXCISOR, CONE FISCHER BIOPSY WD ANGL SM (5/BX) Model Number: 900-157
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1631-2022·2022-08-31
Cooper Surgical Milex Pessary Recalled for Temperature Exposure During Storage
Mckesson Medical-Surgical is recalling Cooper Surgical Milex Pessary Ring products stored at elevated temperatures from June through August 2021, which may have degraded product effectiveness.
Product
COOPER SURGICAL Milex PESSARY, RING MILEX INCONT FLEXIBLE SZ6 1 3/4" Catalog # MXPCON06
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1599-2022·2022-08-31
Merit Medical Systems Aspira Kits Recalled Due to Temperature Excursions
Merit Medical Systems Aspira Dressing and Drainage Kits recalled due to facility temperature excursions from June to August 2021. Exposure to higher temperatures may have reduced product effectiveness; no illnesses reported.
Product
a. MERIT MEDICAL SYSTEMS Aspira Dressing Kit Aspira Model Number: 4991503. b. MERIT MEDICAL SYSTEMS Aspira Pleural / Peritoneal Drainage Kit Aspira 1000 mL Sterile Model Number: 4992301.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1605-2022·2022-08-31
Hydrogen Peroxide Disinfectant Recalled for Potential Loss of Effectiveness
Revital-Ox Resert hydrogen peroxide disinfectant 4-liter containers may have reduced effectiveness due to temperature exposure during storage. McKesson is recalling affected lots distributed June-September 2021.
Product
STERIS CORP Revital-Ox Resert Hydrogen Peroxide High-Level Disinfectant Revital-Ox RESERT RTU Liquid 4 Liter Container Max 21 Day Reuse Model Number: 4455AW
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1635-2022·2022-08-31
Dynarex DynaLube Lubricating Jelly Recalled Due to Temperature Excursions
Mckesson is recalling Dynarex DynaLube lubricating jelly due to facility temperature excursions from June-August 2021 that may have degraded product effectiveness. Recall affects 17.5 boxes distributed nationwide between June-September 2021.
Product
DYNAREX DynaLube LUBRICATING JELLY, STR 2.7GM (144/BX 12BX/CS) Catalog #1250
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1596-2022·2022-08-31
FDA Recalls Heparin Sodium Prefilled Syringes Due to Heat Damage
Mckesson Medical-Surgical Inc. is recalling Excelsior Heparin Sodium prefilled syringes that may have been damaged by temperature excursions during manufacturing, potentially affecting their effectiveness. The recall covers lots received between June and September 2021.
Product
Excelsior Heparin Sodium, Porcine, Preservative Free 100 U / mL Solution Prefilled Syringe, Partial Fill 5 mL Fill in 10 mL Syringe Model Number: 513604
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1636-2022·2022-08-31
Fisher Scientific Swabs Recalled for Temperature Excursion During Storage
Mckesson Medical-Surgical Inc. is recalling Fisherbrand laboratory swabs due to facility temperature excursions from June through August 2021 that may have impacted product effectiveness. All affected lots distributed between June 1 and September 30, 2021 are included.
Product
FISHER SCIENTIFIC Fisherbrand SWAB, ROUND BOTTOM CLR (50/PK)FSHSCI Catalog # 1490712
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1589-2022·2022-08-31
Drugs of Abuse Test Kits Recalled Due to Temperature Exposure
McKesson Medical-Surgical is recalling multiple brands of drugs of abuse test kits because temperature excursions prior to delivery may have reduced product effectiveness.
Product
Drugs of Abuse Tests: a. Wondfo Tdip Drugs of Abuse Test Tdip Single Drug Fentanyl (FEN) Urine Sample 25 Tests. Model Number: AWFTY-114. b. Alere Drugs of Abuse Test E-Z Split Key Cup 12-Drug Panel AMP, BAR, BUP, BZO, COC, mAMP/MET, MDMA, MOP, MTD, OXY, PPX, THC Urine S
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1637-2022·2022-08-31
Total-Fix parasitology stool collection kit recalled for temperature exposure
Mckesson is recalling a Total-Fix stool collection parasitology kit due to temperature exposure that may have reduced its effectiveness. All lots received between June 1 and September 30, 2021 are affected.
Product
MEDICAL CHEMICAL CORPORATION Total-Fix STOOL COLL KIT, TOTAL FIX PARASITOLOGY (100/CS) Catalog # NC0585129
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1624-2022·2022-08-31
Fisher Scientific Sure-Vue Pipette Recall Due to Temperature Exposure
Mckesson Medical-Surgical is recalling Fisher Scientific Sure-Vue RPR Dispensing Pipettes due to temperature excursions during storage from June to August 2021. Exposure to higher temperatures may have impacted product effectiveness.
Product
FISHER SCIENTIFIC Sure-Vue PIPETTE, RPR DISPENSING (500/PK) Catalog # 23038015
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1618-2022·2022-08-31
BD Vacutainer Blood Collection Tubes Recalled for Temperature-Exposure Effectiveness Loss
BD Vacutainer blood collection tubes are recalled due to potential temperature damage during storage from June to August 2021. Affected tubes received between June 1 and September 30, 2021 may have reduced effectiveness.
Product
a. BECTON DICKINSON BD Vacutainer SST TUBE, BLD COL CLOT/SEP GLD 3.5ML PLAS VACUTAINER (100/BX), Model Number: 367983. b. BECTON DICKINSON BD Vacutainer SST TUBE, BLD COL CLOT/SEP RED/GRY8.5ML PLAS VACUTAINER (100/BX Model Number: 367988. c. BECTON DICKINSON BD Vacutaine
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1614-2022·2022-08-31
McKesson and Metrex Research Glutaraldehyde Disinfectants Recalled Due to Temperature Excursion
McKesson and Metrex Research are recalling glutaraldehyde disinfectants due to facility temperature excursions from June to August 2021 that may have reduced product effectiveness. Affected lots were distributed nationwide between June 1 and September 30, 2021.
Product
a. McKesson DISINFECTANT, GLUTARALDEHYDE 28DAY (4GL/CS) MGM68, Model Number: 68-102800. b. METREX RESEARCH McKesson 14-Day Glutaraldehyde Solution DISINFECTANT, GLUTARALDEHYDE 14DAY (4GL/CS) MGM68 Model Number: 68-101400. c. METREX RESEARCH McKesson SOLUTION, GLUT 2.5%
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1600-2022·2022-08-31
Temno Soft Tissue Biopsy Device Recalled for Temperature Exposure
Merit Medical Systems Temno soft tissue biopsy devices may have lost effectiveness due to storage temperature excursions between June and August 2021. The recall affects all lots received between June 1 and September 30, 2021.
Product
MERIT MEDICAL SYSTEMS Temno Soft Tissue Biopsy Device Temno 14 Gauge 6 cm Length Beveled Sharp Tip Model Number: T146
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1610-2022·2022-08-31
Medline Catheter Plugs Recalled for Potential Temperature Exposure Impact
Mckesson Medical-Surgical is recalling Medline catheter plugs (Model DYND12200) due to temperature excursions that may have impacted effectiveness. All lots received between June 1 and September 30, 2021 are affected.
Product
MEDLINE INDUSTRIES Medline Plug, Catheter Medline Plastic, with Cover Model Number: DYND12200
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1598-2022·2022-08-31
Strep A Test Kits Recalled for Potential Temperature Damage
Multiple Strep A diagnostic test kits are being recalled due to temperature exposure during manufacturing and storage that may have compromised test accuracy. All lots received between June 1 and September 30, 2021 are affected.
Product
Strep test: a. McKesson Medical-Surgical McKesson Rapid Test Kit McKesson Consult Infectious Disease Immunoassay Strep A Test Throat / Tonsil Saliva Sample 25 Tests, Model Number: 5003. b. QUIDEL Sofia TEST KIT, STREP A+ SOFIA (25/KT 12KT/CS) Model Number: 20274. c. Alere
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1603-2022·2022-08-31
DisCide Ultra Surface Disinfectant Recalled Due to Temperature Exposure
McKesson Medical-Surgical's DisCide Ultra Surface Disinfectant Cleaner is being recalled because temperature excursions may have reduced product effectiveness. The recall affects all lots distributed nationwide between June and September 2021.
Product
Palmero Healthcare, LLC DisCide Ultra Surface Disinfectant Cleaner Quaternary Based Manual Pour Liquid 1 gal. Jug Herbal Scent NonSterile Model Number: 3565G
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1633-2022·2022-08-31
Dynarex Cotton Swabs Recalled Due to Temperature Exposure
Mckesson Medical-Surgical is recalling Dynarex cotton swabs (197 boxes) received June 1–September 30, 2021, due to temperature excursions during storage that may have reduced product effectiveness.
Product
DYNAREX Dynarex SWABSTICK, PVP (3/PK 25/BX 10BX/CS) Catalog #1202
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1587-2022·2022-08-31
McKesson Pregnancy Test Kits Recalled for Temperature Exposure During Storage
McKesson recalls hCG pregnancy test kits nationwide due to facility temperature excursions that may have compromised product effectiveness. Affected lots were received between June and September 2021.
Product
a. McKesson Rapid Test Kit McKesson Consult Fertility Test hCG Pregnancy Test Serum / Urine Sample 25 Tests. Model Number: 5002. b. McKesson Consult Rapid Test Kit McKesson Consult Fertility Test hCG Pregnancy Test Urine Sample 25 Tests Model Number: 5000. c. McKesso
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1611-2022·2022-08-31
IV Securement Kit Recall Due to Storage Temperature Damage
McKesson is recalling Medline Centurion IV Securement Kits that were exposed to high temperatures during storage, which may have impacted product effectiveness. No illnesses have been reported.
Product
MEDLINE INDUSTRIES Centurion IV Securement Kit Model Number: IVSSTK3
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1616-2022·2022-08-31
B. Braun Anesthesia Support Tray Temperature Excursion Recall
B. Braun Medical Inc. is recalling Anesthesia Support Trays distributed between June and September 2021 due to temperature excursions during storage that may have affected product effectiveness.
Product
B. BRAUN MEDICAL INC. Anesthesia Support Tray SUPPORT TRAY, +EXT SET(10/CS)ST200E Model Number: 332116
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1627-2022·2022-08-31
Medical device swab recall: Fisherbrand SWAB TRANS STUARTS
Mckesson Medical-Surgical initiated a voluntary nationwide recall of Fisherbrand SWAB TRANS STUARTS swabs. The specific reason for the recall is not documented in the FDA notice.
Product
FISHER SCIENTIFIC Fisherbrand SWAB TRANS STUARTS DBL 50BX Catalog #1490721
Category
Medical Device
Distribution
Distributed nationwide