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BLACK SERIES CAMPERS

BLACK SERIES CAMPERS Recalls

All product recalls associated with BLACK SERIES CAMPERS.

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Recall Summary

Total Recalls

1000

Past Year

579

Class I (Serious)

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 3381–3400 of 10937 recalls

Black Series HQ15 Camper (Black Series) – Trailer Equipment Risk (2021)

Fire/Burn Risk

Black Series Campers Inc. (Black Series) is recalling certain 2020-2021 C12, C13, C15, HQ12, HQ15, HQ17, HQ19, HQ19T, HQ21, and HQ22T trailers equipped with Curt emergency breakaway kits, part numbers 52041 and 52044. When the breakaway system pin is pulled and not replaced, the system battery may become depleted and draw electricity through the main battery. This can overload the electrical system.

Moderate

NHTSAFeb 25, 2021Nationwide• BLACK SERIES CAMPERS

Addressable Pull Stations (Potter Electric) – Fire Alert Failure (2021)

Fire/Burn Risk

This recall involves Potter Electric Addressable Pull Stations. When manually pulled, these red-colored devices are intended to activate a fire alarm in commercial and other buildings. Recalled models include: (1) Potter Electric Addressable Dual Action Pull Station, Model PAD100-PSDA, Part Number 3992720, with a date code Dec 03 2020; and (2) Potter Electric Addressable Single Action Pull Station, Model PAD100-PSSA, Part Number 3992721, with date codes Nov 10 2020, Nov 25 2020, Dec 01 2020, and Dec 03 2020. "Potter" is printed on the front of all devices. The date code is located inside the device.

High

CPSCFeb 24, 2021Nationwide

1...168 169170171 172...547

Page 170 of 547Next

• Potter Electric Signal Company, LLC, of St. Louis, Mo.

Smart Port CT Implantable Port (Angiodynamics) – Potential Concerns (2021)

AngioDynamics, Inc. is recalling a specific batch of AngioDynamics Implantable Infusion Port kits and Valved introducers that may have potential for compromised sterility of the device. Only the specific product/lot of the kit identified below is affected by this recall action. The Product Description, Product Number, Ref./Catalog Number and Batch/Lot number is provided below. No other products are affected by this recall.

High

FDAFeb 22, 2021Nationwide• Angiodynamics Inc. (Navilyst Medical Inc.)

BeneVision Monitoring System (Mindray) – Intermittent Freeze Risk (2021)

BeneVision DMS may intermittently freeze and require a manual reboot after which normal operation resumes. If a freeze occur, patients monitored on a telemetry transmitter will no longer communicate data to the BeneVision DMS

High

FDAFeb 22, 2021Nationwide• Mindray DS USA, Inc. dba Mindray North America

Safe Sheath Ultralite (Angiodynamics) – Potential Concerns (2021)

High

FDAFeb 22, 2021Nationwide• Angiodynamics Inc. (Navilyst Medical Inc.)

RayStation Software (RaySearch) – Dose Labeling Error (2021)

For some LINAC types, merging clinical beams with beams of approximate dose may lead to the approximate dose erroneously labeled as clinical dose. Merge beams can be used manually, in scripting, or as part of the Automated breast planning feature. In some cases, when merging two beams where the first beam has clinical dose and the second beam has approximate dose, the dose of the resulting beam will be labeled as Clinical, although dose for some of the beam segments is still calculated with the SVD dose engine and it should be labeled Approximate: Mixed dose. The difference between approximate and final Clinical dose is in most cases small, but there can be body sites such as lung where the difference can be significant.

Low

FDAFeb 22, 2021Nationwide• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

Methylprednisolone Tablets (Jubilant Cadista) – Illegible Label (2021)

Labeling: Illegible label: Customer complaint received of mis-alignment print of the printed dosing instructions on the blister card.

Class IIILow

FDAFeb 19, 2021Nationwide• Jubilant Cadista Pharmaceuticals, Inc.

ThermaCor 1200 Disposable Sets (Smisson-Cartledge) – Aluminum Ion Risk (2021)

Customers are being notified of results from a Toxicological Risk Assessment related to potential for aluminum ions to leach into warmed fluids.

Moderate

FDAFeb 18, 2021Nationwide• Smisson-Cartledge Biomedical, LLC

TASWako Chip Cassette (Fujifilm) – Measurement Inaccuracy (2021)

Potentially defective Chip Cassette units, when used for DCP or AFP-L3% measurement, incorrect DCP and AFP-L3% values may result

High

FDAFeb 18, 2021CA, LA, MN +3 more• Fujifilm Medical Systems U.S.A., Inc.

Operating Table System (Getinge) – Hydraulic Leak Risk (2021)

There is a potential for hydraulic leakage at the inclination function to occur resulting in an unintended Trendelenburg or anti-Trendelenburg movement of the table top depending on patient positioning which may lead to the patient having to be transferred to another OR table causing a delay in the procedure.

High

FDAFeb 11, 2021AL, AK, AZ +39 more• Getinge Group Logistics America, LLC

Impactis NaviKit (Imactis) – Needle Holder Defect (2021)

Defect in the mechanical assembly of the needle holder contained in the navigation kit. One of the 2 jaws of the needle holder does not provide gripping functionality; if the defect is not detected before use, it can cause poor needle guidance and a lack of precision during navigation causing an inaccurate needle position which could cause damage to organs or vasculature adjacent to the trajectory

High

FDAFeb 11, 2021NJ, NY, WI• Imactis 20 Rue Du Tour De L Eau St Martin D Heres France

Muscle Rack Steel Shelving Units (Edsal) – Injury Hazard (2021)

This recall involves Edsal 5-Tier Muscle Rack Heavy Duty Steel Shelving Units used to store heavy items. The units have gray or black-colored steel frames and five plywood shelves. The recalled units include model numbers CR3618, CR3618-BLK, CR4824 and CR4824-BLK. CR3618 and CR3618-BLK are 72 inches in height, 18 inches deep and 36 inches wide. Models CR4824 and CR4824-BLK are 72 inches in height, 24 inches deep and 48 inches wide.

High

CPSCFeb 10, 2021Nationwide• Edsal Manufacturing Company, of Chicago, Ill.

Shannon Percutaneous Burr (In2Bones) – Manufacturing Nonconformity (2021)

This Field Action is being conducted following identification of manufacturing non-conformity of some batches of Shannon burrs diameter 2.0mm length 20mm, possibly causing the breakage of the burr during use.

High

FDAFeb 9, 2021Nationwide• In2Bones, SAS 28 Chemin du petit Bois Ecully France

INFX-8000F System (Canon Medical) – X-Ray Field Shift (2021)

The x-ray irradiation field may shift with respect to image receiving surface displayed on the screen at some C-arm angles.

Moderate

FDAFeb 5, 2021Nationwide• Canon Medical System, USA, INC.

INFX-8000V System (Canon Medical) – X-Ray Field Shift (2021)

The x-ray irradiation field may shift with respect to image receiving surface displayed on the screen at some C-arm angles.

Moderate

FDAFeb 5, 2021Nationwide• Canon Medical System, USA, INC.

INFX-8000C System (Canon Medical) – X-Ray Field Shift (2021)

The x-ray irradiation field may shift with respect to image receiving surface displayed on the screen at some C-arm angles.

Moderate

FDAFeb 5, 2021Nationwide• Canon Medical System, USA, INC.

Panang Curry Sauce (Barbara's Orchard) – Undeclared Shrimp (2021)

Undeclared Allergen

Undeclared allergen: Shrimp

Class IHigh

FDAFeb 5, 2021CO, FL, IL +5 more• Barbara's Orchard/Delicae Gourmet

Thai Peanut Sauce (Barbara's Orchard) – Undeclared Shrimp (2021)

Undeclared Allergen

Undeclared allergen: Shrimp

Class IHigh

FDAFeb 5, 2021CO, FL, IL +5 more• Barbara's Orchard/Delicae Gourmet

Spicy Red Curry Sauce (Barbara's Orchard) – Undeclared Shrimp (2021)

Undeclared Allergen

Undeclared allergen: Shrimp

Class IHigh

FDAFeb 5, 2021CO, FL, IL +5 more• Barbara's Orchard/Delicae Gourmet

Custom Perfusion System (Medtronic) – Bacterial Endotoxin Risk (2021)

Laceration Risk

Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.

High

FDAFeb 4, 2021Nationwide• Medtronic Perfusion Systems