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The Santa Barbara Smokehouse, Inc.

The Santa Barbara Smokehouse, Inc. Recalls

All product recalls associated with The Santa Barbara Smokehouse, Inc..

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Recall Summary

Total Recalls

1000

Past Year

726

Class I (Serious)

175

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 7301–7320 of 11124 recalls

Wild River Pacific Smoked Salmon (Santa Barbara Smokehouse) - Listeria risk (2015)

The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked salmon due to potential Listeria Monocytogenes contamination.

FDAJun 4, 2015AZ, CA, CO +18 more• The Santa Barbara Smokehouse, Inc.

Coastal Harbor Smoked Salmon (Santa Barbara Smokehouse) - Listeria risk (2015)

The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked salmon due to potential Listeria Monocytogenes contamination.

FDAJun 4, 2015AZ, CA, CO +18 more• The Santa Barbara Smokehouse, Inc.

Cambridge House Smoked Salmon – Listeria Risk (2015)

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The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked salmon due to potential Listeria Monocytogenes contamination.

Class IHigh

FDAJun 4, 2015AZ, CA, CO +18 more• The Santa Barbara Smokehouse, Inc.

Balmoral Smoked Salmon – Listeria Risk (2015)

The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked salmon due to potential Listeria Monocytogenes contamination.

FDAJun 4, 2015AZ, CA, CO +18 more• The Santa Barbara Smokehouse, Inc.

Zonisamide 100mg Capsules (American Health) - CGMP investigation (2015)

CGMP Deviations: Firm did not adequately investigate customer complaints.

Class IIModerate

FDAJun 1, 2015Nationwide• American Health Packaging

Azithromycin 500mg Tablets (American Health) - CGMP investigation (2015)

CGMP Deviations: Firm did not adequately investigate customer complaints.

Class IIModerate

FDAJun 1, 2015Nationwide• American Health Packaging

Amlodipine Besylate 10mg Tablets (American Health) - CGMP investigation (2015)

CGMP Deviations: Firm did not adequately investigate customer complaints.

Class IIModerate

FDAJun 1, 2015Nationwide• American Health Packaging

Azithromycin 600mg Tablets (American Health) - CGMP investigation (2015)

CGMP Deviations: Firm did not adequately investigate customer complaints.

Class IIModerate

FDAJun 1, 2015Nationwide• American Health Packaging

Clarithromycin 500mg Tablets (American Health) - CGMP investigation (2015)

CGMP Deviations: Firm did not adequately investigate customer complaints.

Class IIModerate

FDAJun 1, 2015Nationwide• American Health Packaging

Lisinopril 5mg Tablets (American Health) - CGMP investigation (2015)

CGMP Deviations: Firm did not adequately investigate customer complaints.

Class IIModerate

FDAJun 1, 2015Nationwide• American Health Packaging

Azithromycin 250mg Tablets (American Health) - CGMP investigation (2015)

CGMP Deviations: Firm did not adequately investigate customer complaints.

Class IIModerate

FDAJun 1, 2015Nationwide• American Health Packaging

Lisinopril 20mg Tablets (American Health) - CGMP investigation (2015)

CGMP Deviations: Firm did not adequately investigate customer complaints.

Class IIModerate

FDAJun 1, 2015Nationwide• American Health Packaging

Amlodipine Besylate 5mg Tablets (American Health) - CGMP investigation (2015)

CGMP Deviations: Firm did not adequately investigate customer complaints.

Class IIModerate

FDAJun 1, 2015Nationwide• American Health Packaging

Lisinopril 10mg Tablets (American Health) - CGMP investigation (2015)

CGMP Deviations: Firm did not adequately investigate customer complaints.

Class IIModerate

FDAJun 1, 2015Nationwide• American Health Packaging

Lisinopril 40mg Tablets (American Health) - CGMP investigation (2015)

CGMP Deviations: Firm did not adequately investigate customer complaints.

Class IIModerate

FDAJun 1, 2015Nationwide• American Health Packaging

Amlodipine Besylate 2.5mg Tablets (American Health) - CGMP investigation (2015)

CGMP Deviations: Firm did not adequately investigate customer complaints.

Class IIModerate

FDAJun 1, 2015Nationwide• American Health Packaging

Famotidine 20mg Tablets (American Health) - CGMP investigation (2015)

CGMP Deviations: Firm did not adequately investigate customer complaints.

Class IIModerate

FDAJun 1, 2015Nationwide• American Health Packaging

Keystone Carbon (Keystone) – rv equipment risk (2015)

Keystone RV Company (Keystone) is recalling certain model year 2015 Keystone Sprinter, Cougar, Montana, Montana High Country, Outback, Bullet, Avalanche, Alpine, Fuzion, Impact, Laredo, Raptor, Carbon, and Passport, and Dutchmen Kodiak, Aerolite, Denali, and Voltage vehicles. In the affected vehicles, the screws that attach the expanding room to the sliding mechanism cable may fail allowing the room to extend unintentionally while the vehicle is in motion.

NHTSAMay 27, 2015Nationwide• KEYSTONE

Volkswagen Tiguan (Volkswagen) – label placement issue (2015)

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain model year 2015 Tiguan vehicles manufactured January 22, 2015, to March 20, 2015. These vehicles may be equipped with Certification labels that are missing the required tire pressure information and they may state incorrect weight and loading information. As such, these vehicles fail to comply with the requirements of 49 CFR Part 567, "Certification."

NHTSAMay 26, 2015Nationwide• VOLKSWAGEN

Kenworth T680 (Kenworth) – driveshaft problem (2015)

PACCAR Incorporated (PACCAR) is recalling certain model year 2014 and 2015 Kenworth T660, T680, and T800 trucks manufactured January 29, 2013, to April 2, 2014, and 2013 Peterbilt 587 trucks manufactured on August 8, 2012. The affected trucks are built with a driveshaft that may not transmit power to the wheels due to weld failure from corrosion.

NHTSAMay 26, 2015Nationwide• KENWORTH