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Becton Dickinson & Company

Becton Dickinson & Company Recalls

All product recalls associated with Becton Dickinson & Company.

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Recall Summary

Total Recalls

950

Past Year

56

Class I (Serious)

39

Most Recent

Dec 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 361–380 of 950 recalls

Becton Dickinson & Company: PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gau...

Iincorrectly packaged without the required lidocaine as labeled

FDAMar 17, 2020AZ, CT, GA +11 more• Becton Dickinson & Company

Boddingtons Plastics Ltd Wheelbarrow Park Estate Pattenden Lane Tonbridge United Kingdom: Endocuff Vision: models ARV 110, 120, 130, 140 Intende...

Updated Instructions For Use- to contraindications and potential complications/adverse events of the colonoscopy procedure (without using Endocuff Vision Device)

FDAMar 11, 2020Nationwide• Boddingtons Plastics Ltd Wheelbarrow Park Estate Pattenden Lane Tonbridge United Kingdom

ReStructure Vanilla Protein Powder (New Capstone) - Missing milk label (2020)

The firm was notified that the labeling does not include the word milk on the ingredient statement

1...17 181920 21...48

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High

FDAMar 2, 2020Nationwide• New Capstone, Inc

2020 KEYSTONE BULLET Recall: STRUCTURE:EMERGENCY:ESCAPE/EGRESS/EXIT

Keystone RV Company (Keystone) is recalling certain 2020 Bullet 34RI trailers equipped with overhead cabinets across the rear wall. The trailers may be missing an egress window in the main living area, preventing passenger exit in the event of an emergency.

NHTSAFeb 27, 2020Nationwide• KEYSTONE

Becton Dickinson & Company: BARD MYPICC KIT 3F Single-Lumen, Catalog Number CK000417B

The kits contain surgical gowns which were subject to a recall by the supplier.

FDAFeb 26, 2020IN, MO, OH +1 more• Becton Dickinson & Company

Becton Dickinson & Company: BARD MYPICC KIT 5F Triple-Lumen, Catalog Number CK000026A

The kits contain surgical gowns which were subject to a recall by the supplier.

FDAFeb 26, 2020IN, MO, OH +1 more• Becton Dickinson & Company

Becton Dickinson & Company: BARD MYPICC KIT 5F Dual-Lumen, Catalog Number CK000025

The kits contain surgical gowns which were subject to a recall by the supplier.

FDAFeb 26, 2020IN, MO, OH +1 more• Becton Dickinson & Company

Becton Dickinson & Company: BARD MYPICC KIT 4F Single-Lumen, Catalog Number CK000276

The kits contain surgical gowns which were subject to a recall by the supplier.

FDAFeb 26, 2020IN, MO, OH +1 more• Becton Dickinson & Company

Becton Dickinson & Company: BARD MYPICC KIT 4F Dual-Lumen, Catalog Number CK000418B

The kits contain surgical gowns which were subject to a recall by the supplier.

FDAFeb 26, 2020IN, MO, OH +1 more• Becton Dickinson & Company

2020 KEYSTONE CROSSROADS ZINGER Recall: EQUIPMENT:RECREATIONAL VEHICLE/TRAILER

Keystone RV Company (Keystone) is recalling certain 2020 Hideout, Springdale, and Crossroads Zinger trailers. The spare tire carrier U-bolts may fail allowing the spare tire carrier and spare tire detach from the vehicle.

NHTSAFeb 25, 2020Nationwide• KEYSTONE

Walk Behind Leaf Blowers (DR Power) – Projectile hazard (2020)

This recall involves DR Walk Behind Leaf Blowers, including DR PREMIER 1200, DR PRO 2000 and DR PRO 2000SP. The blowers are three-wheeled walk behind blowers with an orange circular metal face with a black center with "DR" printed on the front. The model number is printed on the front left side of the main impeller housing and on the serial number label located on the back right side of the main impeller housing. Only the following models are included in the recall: Product name Model Number DR PREMIER 1200 Walk Behind Leaf Blower WB13010DMN DR PRO 2000 Walk Behind Leaf Blower WB15020DMN DR PRO 2000 Walk Behind Leaf Blower WB15020DEN DR PRO 2000SP Walk Behind Leaf Blower WB17020DEN

CPSCFeb 6, 2020Nationwide• Country Home Products Inc., d/b/a DR Power Equipment, of South Burlington, Vt.

T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Kibbutz Gatton Naharia Israel: FlipCutter III Drill

There is potential for the blister tray to be cracked causing the sterile barrier to be compromised and potential for particulate within the sterile barrier.

FDAJan 20, 2020Nationwide• T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Kibbutz Gatton Naharia Israel

Ranitidine Tablets 150mg (Denton Pharma) – NDMA impurity (2019)

CGMP Deviations: Presence of NDMA impurity detected in product.

Class IIModerate

FDADec 20, 2019Nationwide• Denton Pharma, Inc.

Ranitidine 300mg Tablets (Denton Pharma) – NDMA Impurity (2019)

CGMP Deviations: Presence of NDMA impurity detected in product.

Class IIModerate

FDADec 20, 2019Nationwide• Denton Pharma, Inc.

2020 KEYSTONE SPRINGDALE Recall: EQUIPMENT:OTHER:LABELS

Keystone RV Company (Keystone) is recalling certain 2020 Springdale trailers, models 1700FQ, 1750RD, 1760BH, 1790FQ, and 1800BH. The Federal Identification Tag lists incorrect rim size, tire size, and tire pressure information. As such, these vehicles fail to comply with the requirements of 49 CFR Part 567, "Certification."

NHTSADec 10, 2019Nationwide• KEYSTONE

Flounder with Crabmeat Stuffing (Slade Gorton) – Listeria Risk (2019)

Product stuffing may be contaminated with Listeria monocytogenes

Class IIModerate

FDADec 3, 2019ME, NY, OH +1 more• Slade Gorton & Company, Inc.

Gourmet Bay Salmon Roast (Slade Gorton) – Listeria contamination (2019)

Product stuffing may be contaminated with Listeria monocytogenes

Class IIModerate

FDADec 3, 2019ME, NY, OH +1 more• Slade Gorton & Company, Inc.

Gourmet Bay Haddock (Slade Gorton) – Listeria contamination (2019)

Product stuffing may be contaminated with Listeria monocytogenes

Class IIModerate

FDADec 3, 2019ME, NY, OH +1 more• Slade Gorton & Company, Inc.

Grown In Idaho Hash Browns (Lamb Weston) – hard rubber pieces (2019)

Crispy Hash Brown Dices product is recalled because it may contain pieces of hard rubber material.

Class IIModerate

FDANov 20, 2019AZ, CA, CO +13 more• Lamb Weston Inc

Medtronic Navigation, Inc.-Littleton: O-arm" O2 Imaging System, Product Number/CFN: BI-700-02000

Due to a manufacturing issue affecting particular O-arm" O2 Imaging Systems, Medtronic has determined that the gantry tractor motor drive belt may loosen over an extended number of uses at a higher frequency in these systems. If the belt loosens, it may result in rotation of 3D images about the gantry isocenter. While the 3D image is anatomically accurate within the image itself and may be used to confirm therapy, its electronic registered location may be rotated relative to the actual physical position of the patient.

FDANov 15, 2019AR, CA, CO +24 more• Medtronic Navigation, Inc.-Littleton