Various SRI Surgical Disposable Accessory Packs
Medical device recall Z-2300-2012. Published in FDA’s Enforcement Report on Sep 5, 2012.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Sep 5, 2012. Copied from openFDA on Oct 24, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Nationwide FDA’s word, and 14 states named
- 802,135 how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
Distribution of a product that did not meet specifications. (labeling error)
FDA, Device recall enforcement reports. Released Oct 23, 2026. Updated weekly.
Which ones are recalled?
Various SRI Surgical Disposable Accessory Packs. SRI’s Disposable Accessory Packs (also commonly known as convenience kits and custom procedure trays) are an assembly of medical devices packaged together according to the customer specifications, which are then wrapped in a sterilization wrap and sterilized. This allows the customer to open one package for a surgical procedure instead of many individual packages.
802,135, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 23, 2026. Updated weekly.
Codes to check against yours
Model Numbers: CY1020 GY1250 GY1274 GY1274A GY1274B GY1274C GS1296 NU1290 OR1288 OR1288A OR1289 GS0880C GS0880D GS0880E GS0880F LD0994D LD1000A GS0983C LD1019A LD1019B LD1029A OR0986B OR0986C OR0986D GS0935B-M GY1223 GY1223A CY1028C…
Every code shown here, 1,997 characters
Model Numbers: CY1020 GY1250 GY1274 GY1274A GY1274B GY1274C GS1296 NU1290 OR1288 OR1288A OR1289 GS0880C GS0880D GS0880E GS0880F LD0994D LD1000A GS0983C LD1019A LD1019B LD1029A OR0986B OR0986C OR0986D GS0935B-M GY1223 GY1223A CY1028C CY1028D ET1023A ET1023B ET1023C ET1023D EY1024A EY1024B EY1024C EY1024D EY1024E GS0764D GS0764E GS0780D GS0780E GS1219 LD1022B LD1022C LD1022D LD1132 LD1132A LD1132B OR1025A GS1043 GS1044 GS0937D GS0937E GS0938B GS0938C GS0995 GS0995A GS0995B GS0995C GY0996 HT0980A HT0980B HT0980C HT0987B HT0987C HT1128 NU0939C NU0939D GS1136 GS1136A GS1136B CL1035 CL1035A CL1035B NU0700G ET1243 ET1243A EY1242 GS1200A GS1245 GS1245B GS1248 GS1248A GS1285 GS1285A GS1285B HT1247 HT1247A HT1247B NU1249 NU1249A NU1249B NU1249C OR1196B OR1244 OR1244A OR1244B OR1244C OR1246 OR1246A OR1246B CL0705F CL0705G CL0705H EY0696E HT0482E HT0482F HT0482G HT1228 HT1234A-M HT1234B-M HT1234D-M HT1234E-M HT1234F-M HT1234-M LD0693F LD0693G LD0694C NU0700I NU1157 NU1157A GS1268 GS1268A GS1268C GS1287 GS1287A GS1287B GF1333 GF1333A OR1340 CV0691G CV0691H CY0695G CY0695H CY0695I ED0704K ED0704L ED0704M EY0707F EY0707G GS0689A GS0689C GS0692I GS0692J GS0692K GS0692L GS0697E GS1074 GS1074A GS1074B HT0482I HT0482J HT0482K HT0706B HT0706C NU0690H NU0690I NU0690J NU0690K NU0690L NU0699I NU0699J NU0699K NU0700H OR0698F OR0698G OR0698H OR0925A GS1146 GS1146A GS1147 GY1151 GY1151A OR1148 OR1149 OR1149A OR1150 GS0891C GS0891D CV1186 CV1186A CV1199 ET1197 ET1197A EY1154 EY1183 EY1183A EY1183B EY1183C GS1185 GS1191 GS1193 GS1193A GS1194 GS1194A GS1195 GS1198 GS1200 HT1182 HT1182A HT1182B-M HT1182D LD1301B LD1303 NU1190 NU1190A NU1192 OR1184 OR1184A OR1187 OR1188 OR1188A OR1188B OR1189 OR1196 OR1196A OR1196B OR1263 CL0753C-M CL0753D-M CL0753E CL0753F CL1215 CL1215A CL1215B HT0756H HT0756I HT0756J CL0753G CL0753H CL0753I CL1215A HT0756K BS1209 BS1209A BS1209B CL1253 CL1253A CV1068 CV1069 CY1078 CY1078A CY1078B CY1078C ET1076A ET1076B ET1076C ET1079 ET1079A ET1080A ET1080B EY1077 EY1077A…
FDA’s list runs to 9,592 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Nationwide Distribution-including the states of CA, FL, GA, KY, MD, MI, NC, NJ, OK, PA, SC, TN, TX, and UT.
The states and territories these words name
14 states and territories.
Every one of them
- California
- Florida
- Georgia
- Kentucky
- Maryland
- Michigan
- North Carolina
- New Jersey
- Oklahoma
- Pennsylvania
- South Carolina
- Tennessee
- Texas
- Utah
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Jul 16, 2008.
- FDA classified it on Aug 29, 2012.
- FDA’s Enforcement Report published it on Sep 5, 2012.
- FDA terminated it on Sep 10, 2012.
FDA, Device recall enforcement reports. Released Oct 23, 2026. Updated weekly.
Who is recalling it?
- SRI Surgical, of Tampa, FL.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 23, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 9,592 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 23, 2026 and checked Oct 23, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 24, 2026.