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Retractable Technologies, Inc.

Retractable Technologies, Inc. Recalls

All product recalls associated with Retractable Technologies, Inc..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

Most Recent

Jan 2026

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 4321–4340 of 37665 recalls

EasyPoint Needle (Retractable) – Detachment Risk (2024)

The needle cannula of a retractable needle may detach from the needle holder in the patient.

High

FDAFeb 5, 2024Nationwide• Retractable Technologies, Inc.

Aveir Leadless Pacemaker (Abbott) – Interference Risk (2024)

Their is a potential that electromagnetic interference may cause leadless pacemaker may result in mode change.

Moderate

FDAFeb 5, 2024Nationwide• Abbott Medical

Mesalamine Capsules (Sun Pharmaceutical) – Dissolution Failure (2024)

Failed Dissolution Specifications: Out of specification for dissolution.

Class IIModerate

FDA

1...215 216217218 219...1884

Page 217 of 1884Next

Feb 5, 2024

Nationwide

• SUN PHARMACEUTICAL INDUSTRIES INC

Crumbled Cotija (Castle) – Listeria Risk (2024)

Listeria

Product has the potential to be contaminated with Listeria monocytogenes.

Class IHigh

FDAFeb 5, 2024CA, CT, FL +4 more• Castle Importing, Inc.

Three Cheese Blend (Castle) – Listeria Risk (2024)

Listeria

Product has the potential to be contaminated with Listeria monocytogenes.

Class IHigh

FDAFeb 5, 2024CA, CT, FL +4 more• Castle Importing, Inc.

Cerebase DA Guide Sheath (Medos) – Fracture Risk (2024)

Medos has received an increase in complaints for CEREBASE DA Guide Sheath with reports of fractures at the distal end, which may result in surgical procedural delay, vascular injury and in extreme rare occasions it may result in embolism.

High

FDAFeb 2, 2024Nationwide• Medos International Sarl Chemin Blanc 36 Le Locle Switzerland

Forest River Wildwood (Forest River) – Incorrect Label (2024)

Forest River, Inc. (Forest River) is recalling certain 2023-2024 Salem and Wildwood fifth wheel travel trailers. The Federal Placard may have incorrect tire size information. As such, these trailers fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 120, "Wheels and Rims - Other Than Passenger Cars."

Moderate

NHTSAFeb 2, 2024Nationwide• FOREST RIVER

Gulf Stream Trail Boss (Gulf Stream) – Incorrect Label (2024)

Gulf Stream Coach, Inc. (Gulf Stream) is recalling certain 2024 Trail Boss 160FK trailers. The incorrect tire size and tire pressure are listed on the federal certification label. As such, these trailers fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 110, "Tire Selection and Rims" and 49 CFR Part 567, "Certification."

Moderate

NHTSAFeb 2, 2024Nationwide• GULF STREAM

Omeprazole Suspension (Bausch Health) – Subpotent Drug (2024)

Subpotent Drug: Out of specification for assay

Class IIModerate

FDAFeb 2, 2024Nationwide• Bausch Health Companies, Inc.

Visitec Irrigation Handle (Beaver) – Missing Label Info (2024)

Pack and pouch label is missing the manufacturing and expiration date.

Low

FDAFeb 2, 2024Nationwide• Beaver Visitec International, Inc.

M1000 Wash Station (Abbott) – Export Specification Mismatch (2024)

Products that were intended for export only which were not approved or registered in accordance with U.S. specifications were shipped to U.S. customers.

Low

FDAFeb 1, 2024Nationwide• Abbott Molecular, Inc.

Vysis MDM2 FISH Probe Kit (Abbott) – Export Specification Mismatch (2024)

Products that were intended for export only which were not approved or registered in accordance with U.S. specifications were shipped to U.S. customers.

Low

FDAFeb 1, 2024Nationwide• Abbott Molecular, Inc.

Spinach & Feta Croissant (Frothy Monkey) – Metal Fragments (2024)

Potential Foreign Material - Metal Fragments

Class IIModerate

FDAFeb 1, 2024AL, TN• Bakery by Frothy Monkey

HydrALAZINE Tablets (Amerisource) – Impurities Specification (2024)

Failed Impurities/Degradation Specifications: Out of Specification (OOS) result in the repackaged product for Related Compounds (Impurities) at the 6-month time point.

Class IIILow

FDAFeb 1, 2024Nationwide• Amerisource Health Services LLC

TING Tolnaftate Spray (Insight) – Benzene Contamination (2024)

Chemical Contamination; presence of benzene.

Class IHigh

FDAFeb 1, 2024Nationwide• Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company

To the Moon Capsules (Integrity) – Undeclared Sildenafil (2024)

Undeclared Allergen

Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.

Class IHigh

FDAFeb 1, 2024Nationwide• Integrity Products

Lansoprazole Capsules (NATCO Pharma) – Inadequate Sealing (2024)

CGMP Deviations: Inadequate induction sealing on bottles, capsules were observed with bubbles on band seal, capsules with holes and spheres sticking to capsules. Also coding details were missing on one bottle.

Class IIModerate

FDAFeb 1, 2024Nationwide• NATCO Pharma Limited

RAM IT Horny Goat Weed Capsules (Integrity) – Undeclared Sildenafil (2024)

Undeclared Allergen

Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.

Class IHigh

FDAFeb 1, 2024Nationwide• Integrity Products

Entegra Reatta XL (Entegra) – Seat Mounting Defect (2024)

Jayco, Inc. (Jayco) is recalling certain 2020-2023 Entegra Anthem, Aspire, Cornerstone, and Reatta XL motorhomes. The pedestal mounting plate on the passenger's seat may be improperly welded, causing the plate to separate and the seat assembly to loosen or detach. As such, these seat assemblies fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 207, "Seating Systems" and number 210, "Seat belt assembly anchorages."

High

NHTSAFeb 1, 2024Nationwide• ENTEGRA

Plain Croissant (Frothy Monkey) – Metal Fragments (2024)

Potential Foreign Material - Metal Fragments

Class IIModerate

FDAFeb 1, 2024AL, TN• Bakery by Frothy Monkey